12-120636887-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636887
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636887
    reference: chr 12
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.439T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.276+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.401T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1889+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.624+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.318+34T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.399+34T>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-120636894-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636894
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636894
    reference: chr 12
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.276+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.394G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1889+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.258+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.432G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.399+27G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.318+27G>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

12-120636897-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636897
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636897
    reference: chr 12
allele count: 4
allele frequency: 3.299132328197684e-5
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.399+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1889+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.429A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.276+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.391A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.258+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+24A>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+24A>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

12-120636901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636901
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636901
    reference: chr 12
allele count: 225
allele frequency: 1.855394663060329e-3
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.425G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.387G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.258+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.399+20G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.624+20G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-120636906-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636906
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636906
    reference: chr 12
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.276+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.382G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.399+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.258+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.420G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.624+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1889+15G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+15G>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

12-120636908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636908
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636908
    reference: chr 12
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.509+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*155+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.498+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.380T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.360+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1889+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.276+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.418T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.276+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.624+13T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.318+13T>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-120636925-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636925
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636925
    reference: chr 12
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.395A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.314A>G
  hgvsp: ENSP00000339027.3:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.620A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.314A>G
  hgvsp: ENSP00000448046.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.401A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.314A>G
  hgvsp: ENSP00000447311.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.363A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*151A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.314A>G
  hgvsp: ENSP00000450019.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.314A>G
  hgvsp: ENSP00000366471.4:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1885A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.314A>G
  hgvsp: ENSP00000448223.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.505A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.314A>G
  hgvsp: ENSP00000449328.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.254A>G
  hgvsp: ENSP00000449854.1:p.Asn85Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.272A>G
  hgvsp: ENSP00000449765.1:p.Asn91Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.314A>G
  hgvsp: ENSP00000376299.4:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.314A>G
  hgvsp: ENSP00000448639.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.314A>G
  hgvsp: ENSP00000450222.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn105Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

12-120636933-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636933
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636933
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.306G>C
  hgvsp: ENSP00000449205.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.306G>C
  hgvsp: ENSP00000339027.3:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.306G>C
  hgvsp: ENSP00000450222.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.306G>C
  hgvsp: ENSP00000450019.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.264G>C
  hgvsp: ENSP00000450121.1:p.Leu88Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.306G>C
  hgvsp: ENSP00000447311.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.264G>C
  hgvsp: ENSP00000449765.1:p.Leu88Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.393G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.306G>C
  hgvsp: ENSP00000448046.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.306G>C
  hgvsp: ENSP00000376299.4:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.306G>C
  hgvsp: ENSP00000448639.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.612G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.306G>C
  hgvsp: ENSP00000449328.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.355G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.306G>C
  hgvsp: ENSP00000366471.4:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.497G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.387G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1877G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.306G>C
  hgvsp: ENSP00000448223.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu102Phe
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

12-120636952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636952
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636952
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.287C>T
  hgvsp: ENSP00000376299.4:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.287C>T
  hgvsp: ENSP00000449328.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.287C>T
  hgvsp: ENSP00000448046.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.245C>T
  hgvsp: ENSP00000449765.1:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.287C>T
  hgvsp: ENSP00000450222.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.374C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.245C>T
  hgvsp: ENSP00000450121.1:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.368C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.287C>T
  hgvsp: ENSP00000447311.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.287C>T
  hgvsp: ENSP00000450019.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.287C>T
  hgvsp: ENSP00000449205.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.287C>T
  hgvsp: ENSP00000448223.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.478C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.287C>T
  hgvsp: ENSP00000339027.3:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.287C>T
  hgvsp: ENSP00000366471.4:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1858C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.329C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.336C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr96Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-120636957-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636957
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636957
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.324C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.363C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.240C>A
  hgvsp: ENSP00000450121.1:p.Asp80Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.282C>A
  hgvsp: ENSP00000450019.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.222C>A
  hgvsp: ENSP00000449854.1:p.Asp74Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.282C>A
  hgvsp: ENSP00000448046.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.282C>A
  hgvsp: ENSP00000450222.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.282C>A
  hgvsp: ENSP00000376299.4:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.282C>A
  hgvsp: ENSP00000339027.3:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.473C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.282C>A
  hgvsp: ENSP00000449328.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.282C>A
  hgvsp: ENSP00000366471.4:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.282C>A
  hgvsp: ENSP00000449205.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.282C>A
  hgvsp: ENSP00000447311.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.282C>A
  hgvsp: ENSP00000448639.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.282C>A
  hgvsp: ENSP00000448223.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.588C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.240C>A
  hgvsp: ENSP00000449765.1:p.Asp80Glu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.331C>A
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp94Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

12-120636963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636963
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636963
    reference: chr 12
allele count: 860
allele frequency: 7.085187015982864e-3
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.234G>A
  hgvsp: ENST00000550423.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.276G>A
  hgvsp: ENST00000228306.4:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.276G>A
  hgvsp: ENST00000313104.5:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.276G>A
  hgvsp: ENST00000546989.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.276G>A
  hgvsp: ENST00000546990.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.276G>A
  hgvsp: ENST00000392514.4:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.276G>A
  hgvsp: ENST00000550856.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.467G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.276G>A
  hgvsp: ENST00000551914.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.276G>A
  hgvsp: ENST00000547475.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*113G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1847G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.357G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.234G>A
  hgvsp: ENST00000547191.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.216G>A
  hgvsp: ENST00000547211.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.276G>A
  hgvsp: ENST00000551258.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.582G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.318G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.276G>A
  hgvsp: ENST00000547173.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys92Lys
num of homozygotes: 9
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-120636972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636972
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636972
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.309G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.225G>A
  hgvsp: ENST00000547191.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.225G>A
  hgvsp: ENST00000550423.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.267G>A
  hgvsp: ENST00000313104.5:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.267G>A
  hgvsp: ENST00000547475.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.267G>A
  hgvsp: ENST00000551258.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.267G>A
  hgvsp: ENST00000392514.4:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.267G>A
  hgvsp: ENST00000546989.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.267G>A
  hgvsp: ENST00000551914.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.447G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.573G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.267G>A
  hgvsp: ENST00000547173.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.267G>A
  hgvsp: ENST00000228306.4:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.316G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.267G>A
  hgvsp: ENST00000550856.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*104G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.458G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.267G>A
  hgvsp: ENST00000551150.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.673G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val89Val
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-120636981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636981
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636981
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.300G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.664G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.258G>A
  hgvsp: ENST00000392514.4:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.258G>A
  hgvsp: ENST00000546990.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.258G>A
  hgvsp: ENST00000313104.5:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.258G>A
  hgvsp: ENST00000546989.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.258G>A
  hgvsp: ENST00000550856.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.258G>A
  hgvsp: ENST00000551150.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.258G>A
  hgvsp: ENST00000547173.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.258G>A
  hgvsp: ENST00000551258.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.258G>A
  hgvsp: ENST00000228306.4:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.258G>A
  hgvsp: ENST00000547475.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.438G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.339G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.198G>A
  hgvsp: ENST00000547211.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.216G>A
  hgvsp: ENST00000550423.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.345G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.258G>A
  hgvsp: ENST00000551914.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.216G>A
  hgvsp: ENST00000547191.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val86Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

12-120636983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636983
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636983
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.256G>A
  hgvsp: ENSP00000449328.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.214G>A
  hgvsp: ENSP00000450121.1:p.Val72Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*93G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.256G>A
  hgvsp: ENSP00000448639.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.256G>A
  hgvsp: ENSP00000450222.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1827G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.343G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.662G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.256G>A
  hgvsp: ENSP00000448223.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.436G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.196G>A
  hgvsp: ENSP00000449854.1:p.Val66Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.256G>A
  hgvsp: ENSP00000366471.4:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.298G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.256G>A
  hgvsp: ENSP00000448046.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.256G>A
  hgvsp: ENSP00000449205.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.214G>A
  hgvsp: ENSP00000449765.1:p.Val72Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.256G>A
  hgvsp: ENSP00000376299.4:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.256G>A
  hgvsp: ENSP00000447311.1:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.256G>A
  hgvsp: ENSP00000339027.3:p.Val86Met
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val86Met
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-120636984-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636984
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636984
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.255T>C
  hgvsp: ENST00000551258.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.255T>C
  hgvsp: ENST00000547475.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.255T>C
  hgvsp: ENST00000313104.5:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.255T>C
  hgvsp: ENST00000550856.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.213T>C
  hgvsp: ENST00000547191.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.255T>C
  hgvsp: ENST00000228306.4:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.255T>C
  hgvsp: ENST00000546989.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.304T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.255T>C
  hgvsp: ENST00000546990.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.195T>C
  hgvsp: ENST00000547211.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.561T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.255T>C
  hgvsp: ENST00000392514.4:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.255T>C
  hgvsp: ENST00000551150.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1826T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.255T>C
  hgvsp: ENST00000547173.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.213T>C
  hgvsp: ENST00000550423.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.255T>C
  hgvsp: ENST00000551914.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.297T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.336T>C
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn85Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-120636990-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636990
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636990
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1820G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.249G>A
  hgvsp: ENST00000546989.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.249G>A
  hgvsp: ENST00000550856.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.249G>A
  hgvsp: ENST00000551150.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.336G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.207G>A
  hgvsp: ENST00000550423.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.249G>A
  hgvsp: ENST00000551258.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.298G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.429G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.249G>A
  hgvsp: ENST00000313104.5:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.249G>A
  hgvsp: ENST00000392514.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.249G>A
  hgvsp: ENST00000547475.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.555G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.249G>A
  hgvsp: ENST00000546990.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.249G>A
  hgvsp: ENST00000228306.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.249G>A
  hgvsp: ENST00000547173.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.291G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.330G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.207G>A
  hgvsp: ENST00000547191.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg83Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

12-120636992-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636992
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636992
    reference: chr 12
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.205C>T
  hgvsp: ENSP00000449765.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.247C>T
  hgvsp: ENSP00000449205.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.247C>T
  hgvsp: ENSP00000450222.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.247C>T
  hgvsp: ENSP00000376299.4:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.328C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.247C>T
  hgvsp: ENSP00000449328.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.247C>T
  hgvsp: ENSP00000450019.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.187C>T
  hgvsp: ENSP00000449854.1:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1818C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.247C>T
  hgvsp: ENSP00000366471.4:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.334C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.289C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.247C>T
  hgvsp: ENSP00000448639.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.247C>T
  hgvsp: ENSP00000339027.3:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.205C>T
  hgvsp: ENSP00000450121.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.438C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.653C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.247C>T
  hgvsp: ENSP00000447311.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.247C>T
  hgvsp: ENSP00000448223.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg83Trp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-120636996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636996
    reference: chr 12
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.183T>C
  hgvsp: ENST00000547211.1:c.183T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.243T>C
  hgvsp: ENST00000546990.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.434T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.243T>C
  hgvsp: ENST00000313104.5:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.649T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.549T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.243T>C
  hgvsp: ENST00000547475.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.243T>C
  hgvsp: ENST00000547173.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.243T>C
  hgvsp: ENST00000550856.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1814T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.423T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.201T>C
  hgvsp: ENST00000550423.1:c.201T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.243T>C
  hgvsp: ENST00000551258.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.243T>C
  hgvsp: ENST00000546989.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.243T>C
  hgvsp: ENST00000551150.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.243T>C
  hgvsp: ENST00000551914.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.243T>C
  hgvsp: ENST00000392514.4:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.330T>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.292T>C
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His81His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

12-120636998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120636998
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120636998
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.241C>T
  hgvsp: ENSP00000339027.3:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*78C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.241C>T
  hgvsp: ENSP00000449205.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.290C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.322C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.432C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.181C>T
  hgvsp: ENSP00000449854.1:p.His61Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.241C>T
  hgvsp: ENSP00000366471.4:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.241C>T
  hgvsp: ENSP00000450222.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.241C>T
  hgvsp: ENSP00000448639.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.547C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.199C>T
  hgvsp: ENSP00000450121.1:p.His67Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1812C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.241C>T
  hgvsp: ENSP00000448046.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.241C>T
  hgvsp: ENSP00000450019.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.199C>T
  hgvsp: ENSP00000449765.1:p.His67Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.241C>T
  hgvsp: ENSP00000449328.1:p.His81Tyr
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.328C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.283C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His81Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

12-120637000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637000
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637000
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.239C>T
  hgvsp: ENSP00000450222.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.320C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.239C>T
  hgvsp: ENSP00000449328.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.239C>T
  hgvsp: ENSP00000448046.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.239C>T
  hgvsp: ENSP00000339027.3:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.239C>T
  hgvsp: ENSP00000448223.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.288C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*76C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.197C>T
  hgvsp: ENSP00000450121.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.239C>T
  hgvsp: ENSP00000450019.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.239C>T
  hgvsp: ENSP00000449205.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.197C>T
  hgvsp: ENSP00000449765.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.430C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.545C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.239C>T
  hgvsp: ENSP00000447311.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.239C>T
  hgvsp: ENSP00000448639.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.326C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.239C>T
  hgvsp: ENSP00000366471.4:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.281C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro80Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

12-120637002-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637002
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637002
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.195G>C
  hgvsp: ENST00000550423.1:c.195G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.237G>C
  hgvsp: ENST00000228306.4:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.428G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1808G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*74G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.643G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.237G>C
  hgvsp: ENST00000313104.5:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.237G>C
  hgvsp: ENST00000547475.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.237G>C
  hgvsp: ENST00000551150.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.543G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.417G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.237G>C
  hgvsp: ENST00000550856.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.237G>C
  hgvsp: ENST00000546990.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.237G>C
  hgvsp: ENST00000551258.1:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.237G>C
  hgvsp: ENST00000392514.4:c.237G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.195G>C
  hgvsp: ENST00000547191.1:c.195G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.279G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.177G>C
  hgvsp: ENST00000547211.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.286G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.318G>C
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu79Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

12-120637005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637005
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637005
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.234G>A
  hgvsp: ENST00000547475.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.234G>A
  hgvsp: ENST00000546989.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.234G>A
  hgvsp: ENST00000228306.4:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.540G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.234G>A
  hgvsp: ENST00000313104.5:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.315G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.192G>A
  hgvsp: ENST00000550423.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.234G>A
  hgvsp: ENST00000550856.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.234G>A
  hgvsp: ENST00000546990.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.234G>A
  hgvsp: ENST00000392514.4:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.234G>A
  hgvsp: ENST00000551258.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.425G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.283G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.174G>A
  hgvsp: ENST00000547211.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.234G>A
  hgvsp: ENST00000547173.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.640G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.192G>A
  hgvsp: ENST00000547191.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1805G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu78Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/12-120637013-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637013
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637013
    reference: chr 12
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.417T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.406T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-5T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-5T>G
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.231-5T>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

12-120637018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637018
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637018
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.401C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.412C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.627C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-10C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-10C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

12-120637021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637021
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637021
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.624C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.409C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.398C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-13C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-13C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

12-120637028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637028
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637028
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.402C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.617C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.391C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-20C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-20C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

12-120637039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637039
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637039
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.391G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.606G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.380G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-31G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-31G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

12-120637046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637046
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637046
    reference: chr 12
allele count: 184
allele frequency: 1.515875500486069e-3
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.373C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.384C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.599C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-38C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-38C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS

12-120637049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637049
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637049
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.596G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.370G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.381G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-41G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-41G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

12-120637050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637050
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637050
    reference: chr 12
allele count: 11
allele frequency: 9.061701952384875e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.595G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.380G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.369G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-42G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-120637054-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637054
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637054
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.591G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.365G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.376G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-46G>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-46G>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

12-120637056-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637056
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637056
    reference: chr 12
allele count: 44
allele frequency: 3.624800224078559e-4
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.589G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.363G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.374G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-48G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-48G>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

12-120637059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637059
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637059
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.586C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.371C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.537-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.360C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.280-51C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*68-51C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-120637060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637060
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637060
    reference: chr 12
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.359C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.370C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.273-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.585C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.171-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1802-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.231-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.189-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.318-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.189-52C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.312-52C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-120637063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637063
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637063
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.356C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.367C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.582C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+50C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+50C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

12-120637063-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637063
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637063
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.582C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.356C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.367C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+50C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+50C>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

12-120637068-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637068
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637068
    reference: chr 12
allele count: 8
allele frequency: 6.589785831960461e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.351T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.362T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.577T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+45T>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+45T>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-120637069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637069
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637069
    reference: chr 12
allele count: 6
allele frequency: 4.942420797706717e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.350C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.576C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.361C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+44C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+44C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-120637071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637071
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637071
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.574G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.359G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.348G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+42G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+42G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

12-120637072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637072
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637072
    reference: chr 12
allele count: 16
allele frequency: 1.318000593100267e-4
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.347C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.573C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.358C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+41C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+41C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-120637072-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637072
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637072
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.358C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.347C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.573C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+41C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+41C>G
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

12-120637074-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637074
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637074
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.345C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.356C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.571C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+39C>A
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

12-120637079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637079
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637079
    reference: chr 12
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.340C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.351C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.566C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+34C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+34C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-120637080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637080
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637080
    reference: chr 12
allele count: 9
allele frequency: 7.414364094706144e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.350C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.339C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.565C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+33C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+33C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

12-120637081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637081
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637081
    reference: chr 12
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.338C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.349C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.564C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+32C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+32C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-120637084-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637084
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637084
    reference: chr 12
allele count: 12
allele frequency: 9.884515905833511e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.561C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.346C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.335C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+29C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+29C>G
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

12-120637088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637088
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637088
    reference: chr 12
allele count: 18
allele frequency: 1.482677385875027e-4
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.557C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.331C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+25C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+25C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-120637093-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637093
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637093
    reference: chr 12
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.552T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.326T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.337T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+20T>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+20T>G
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

12-120637096-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637096
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637096
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.334G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.549G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.323G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+17G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+17G>C
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

12-120637102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637102
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637102
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.188+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.543C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.170+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.328C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.317C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.230+11C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+11C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-120637105-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637105
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637105
    reference: chr 12
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.272+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.311+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.317+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.536+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.314C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.279+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*67+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.325C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1801+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.188+8C>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.230+8C>A
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.230+8C>A
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff

12-120637115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637115
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637115
    reference: chr 12
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.228G>A
  hgvsp: ENST00000228306.4:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.228G>A
  hgvsp: ENST00000546990.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.277G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.309G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.228G>A
  hgvsp: ENST00000551914.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.186G>A
  hgvsp: ENST00000547191.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.534G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.315G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.228G>A
  hgvsp: ENST00000550856.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.228G>A
  hgvsp: ENST00000392514.4:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.228G>A
  hgvsp: ENST00000547173.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.315G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.228G>A
  hgvsp: ENST00000547475.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.270G>A
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.228G>A
  hgvsp: ENST00000551258.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.228G>A
  hgvsp: ENST00000313104.5:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.228G>A
  hgvsp: ENST00000546989.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.530G>A
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.228G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

12-120637120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637120
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637120
    reference: chr 12
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.223C>T
  hgvsp: ENST00000392514.4:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.223C>T
  hgvsp: ENST00000550856.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.223C>T
  hgvsp: ENST00000547173.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.223C>T
  hgvsp: ENST00000313104.5:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.223C>T
  hgvsp: ENST00000546990.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.181C>T
  hgvsp: ENST00000550423.1:c.181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.223C>T
  hgvsp: ENST00000546989.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.529C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.181C>T
  hgvsp: ENST00000547191.1:c.181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1794C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.223C>T
  hgvsp: ENST00000551914.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.223C>T
  hgvsp: ENST00000551258.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.223C>T
  hgvsp: ENST00000547475.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.223C>T
  hgvsp: ENST00000228306.4:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000551783
  gene symbol: RPLP0
  hgvsc: ENST00000551783.1:n.525C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.272C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.310C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.163C>T
  hgvsp: ENST00000547211.1:c.163C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu75Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

12-120637120-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637120
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637120
    reference: chr 12
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.223C>G
  hgvsp: ENSP00000366471.4:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.272C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.163C>G
  hgvsp: ENSP00000449854.1:p.Leu55Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.223C>G
  hgvsp: ENSP00000376299.4:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.223C>G
  hgvsp: ENSP00000450222.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.223C>G
  hgvsp: ENSP00000448639.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.223C>G
  hgvsp: ENSP00000448046.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.223C>G
  hgvsp: ENSP00000449205.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.529C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.310C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.265C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.223C>G
  hgvsp: ENSP00000339027.3:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1794C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.181C>G
  hgvsp: ENSP00000449765.1:p.Leu61Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.223C>G
  hgvsp: ENSP00000447311.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.181C>G
  hgvsp: ENSP00000450121.1:p.Leu61Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*60C>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.223C>G
  hgvsp: ENSP00000450019.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.223C>G
  hgvsp: ENSP00000448223.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu75Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

12-120637127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637127
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637127
    reference: chr 12
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.297C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.216C>T
  hgvsp: ENST00000551914.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.174C>T
  hgvsp: ENST00000547191.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.522C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.216C>T
  hgvsp: ENST00000546989.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.216C>T
  hgvsp: ENST00000551150.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.216C>T
  hgvsp: ENST00000550856.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.174C>T
  hgvsp: ENST00000550423.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.216C>T
  hgvsp: ENST00000547475.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.216C>T
  hgvsp: ENST00000228306.4:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.216C>T
  hgvsp: ENST00000392514.4:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.292C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.216C>T
  hgvsp: ENST00000547173.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.156C>T
  hgvsp: ENST00000547211.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.216C>T
  hgvsp: ENST00000551258.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.216C>T
  hgvsp: ENST00000313104.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.258C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.303C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.303C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn72Asn
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

12-120637146-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637146
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637146
    reference: chr 12
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.239G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.155G>C
  hgvsp: ENSP00000449765.1:p.Arg52Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*34G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.197G>C
  hgvsp: ENSP00000448223.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.197G>C
  hgvsp: ENSP00000448639.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.197G>C
  hgvsp: ENSP00000449205.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.284G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.155G>C
  hgvsp: ENSP00000450121.1:p.Arg52Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.197G>C
  hgvsp: ENSP00000450222.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.246G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.197G>C
  hgvsp: ENSP00000339027.3:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.197G>C
  hgvsp: ENSP00000366471.4:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1768G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.197G>C
  hgvsp: ENSP00000449328.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.503G>C
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.197G>C
  hgvsp: ENSP00000376299.4:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.197G>C
  hgvsp: ENSP00000448046.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.197G>C
  hgvsp: ENSP00000447311.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.278G>C
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg66Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

12-120637151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637151
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637151
    reference: chr 12
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.279C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.192C>T
  hgvsp: ENST00000551258.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.192C>T
  hgvsp: ENST00000546989.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448919
  ensembl transcript: ENST00000549098
  gene symbol: RPLP0
  hgvsc: ENST00000549098.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000339027
  ensembl transcript: ENST00000228306
  gene symbol: RPLP0
  hgvsc: ENST00000228306.4:c.192C>T
  hgvsp: ENST00000228306.4:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.150C>T
  hgvsp: ENST00000547191.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.241C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.192C>T
  hgvsp: ENST00000547173.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.192C>T
  hgvsp: ENST00000313104.5:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.150C>T
  hgvsp: ENST00000550423.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.132C>T
  hgvsp: ENST00000547211.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.192C>T
  hgvsp: ENST00000547475.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.192C>T
  hgvsp: ENST00000550856.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.192C>T
  hgvsp: ENST00000551150.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.192C>T
  hgvsp: ENST00000551914.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.279C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.268C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552461
  gene symbol: RPLP0
  hgvsc: ENST00000552461.1:n.1763C>T
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000546564
  gene symbol: RPLP0
  hgvsc: ENST00000546564.1:n.273C>T
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala64Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

12-120637155-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 120637155
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 120637155
    reference: chr 12
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448223
  ensembl transcript: ENST00000551914
  gene symbol: RPLP0
  hgvsc: ENST00000551914.1:c.188A>G
  hgvsp: ENSP00000448223.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449854
  ensembl transcript: ENST00000547211
  gene symbol: RPLP0
  hgvsc: ENST00000547211.1:c.128A>G
  hgvsp: ENSP00000449854.1:p.Lys43Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449328
  ensembl transcript: ENST00000551150
  gene symbol: RPLP0
  hgvsc: ENST00000551150.1:c.188A>G
  hgvsp: ENSP00000449328.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000366471
  ensembl transcript: ENST00000313104
  gene symbol: RPLP0
  hgvsc: ENST00000313104.5:c.188A>G
  hgvsp: ENSP00000366471.4:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448046
  ensembl transcript: ENST00000550856
  gene symbol: RPLP0
  hgvsc: ENST00000550856.1:c.188A>G
  hgvsp: ENSP00000448046.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449765
  ensembl transcript: ENST00000550423
  gene symbol: RPLP0
  hgvsc: ENST00000550423.1:c.146A>G
  hgvsp: ENSP00000449765.1:p.Lys49Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450121
  ensembl transcript: ENST00000547191
  gene symbol: RPLP0
  hgvsc: ENST00000547191.1:c.146A>G
  hgvsp: ENSP00000450121.1:p.Lys49Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000550296
  gene symbol: RPLP0
  hgvsc: ENST00000550296.1:n.230A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548495
  gene symbol: RPLP0
  hgvsc: ENST00000548495.1:n.275A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000552902
  gene symbol: RPLP0
  hgvsc: ENST00000552902.1:n.494A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548568
  gene symbol: RPLP0
  hgvsc: ENST00000548568.1:n.237A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450222
  ensembl transcript: ENST00000547475
  gene symbol: RPLP0
  hgvsc: ENST00000547475.1:c.188A>G
  hgvsp: ENSP00000450222.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000447311
  ensembl transcript: ENST00000546990
  gene symbol: RPLP0
  hgvsc: ENST00000546990.1:c.188A>G
  hgvsp: ENSP00000447311.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000548551
  gene symbol: RPLP0
  hgvsc: ENST00000548551.1:n.275A>G
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000376299
  ensembl transcript: ENST00000392514
  gene symbol: RPLP0
  hgvsc: ENST00000392514.4:c.188A>G
  hgvsp: ENSP00000376299.4:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000450019
  ensembl transcript: ENST00000547173
  gene symbol: RPLP0
  hgvsc: ENST00000547173.1:c.188A>G
  hgvsp: ENSP00000450019.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000449205
  ensembl transcript: ENST00000546989
  gene symbol: RPLP0
  hgvsc: ENST00000546989.1:c.188A>G
  hgvsp: ENSP00000449205.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089157
  ensembl protein: ENSP00000448639
  ensembl transcript: ENST00000551258
  gene symbol: RPLP0
  hgvsc: ENST00000551258.1:c.188A>G
  hgvsp: ENSP00000448639.1:p.Lys63Arg
  variant of: http://identifiers.org/hgnc/10371
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089157
  ensembl transcript: ENST00000549242
  gene symbol: RPLP0
  hgvsc: ENST00000549242.1:n.264A>G
  variant of: http://identifiers.org/hgnc/10371
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys63Arg
num of homozygotes: 0
reference allele: T

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.258+34T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.318+34T>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 2391
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9726
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8515
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1024
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3649
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1999
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5905
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1610
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 677
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9311
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7534
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5563
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3895
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28881
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7723
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.912e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

VQSLOD
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 2.556066e6

QD
type: SiteQuality
SIO_000300: 1.659e1

MQ
type: SiteQuality
SIO_000300: 5.837e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.108e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450222
ensembl transcript: ENST00000547475
gene symbol: RPLP0
hgvsc: ENST00000547475.1:c.318+27G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.624+27G>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1024
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3650
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1609
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9844
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6090
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5564
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8626
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9341
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7544
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2391
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1999
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4502
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28896
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2703
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4211
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.343e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

DP
type: SiteQuality
SIO_000300: 2.561443e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.657e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.318+24A>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.624+24A>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1607
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9348
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9870
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8661
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6175
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3651
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7552
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2391
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1024
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 679
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5567
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 315
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1999
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 504
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28905
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.001140216641162e-5
allele num: 66654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

VQSLOD
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 2.563364e6

FS
type: SiteQuality
SIO_000300: 1.901e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

QD
type: SiteQuality
SIO_000300: 1.465e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.276+20G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1889+20G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 255
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8687
bin: 2.75e1
variant carriers: 12

GenotypeDepth
all individuals: 287
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 7.75e1
variant carriers: 10

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6136
bin: 2.25e1
variant carriers: 6

GenotypeDepth
all individuals: 1612
bin: 6.25e1
variant carriers: 10

GenotypeDepth
all individuals: 9359
bin: 3.75e1
variant carriers: 19

GenotypeDepth
all individuals: 5574
bin: 4.75e1
variant carriers: 17

GenotypeDepth
all individuals: 7576
bin: 4.25e1
variant carriers: 33

GenotypeDepth
all individuals: 9957
bin: 3.25e1
variant carriers: 19

GenotypeDepth
all individuals: 3657
bin: 5.25e1
variant carriers: 21

GenotypeDepth
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 7.25e1
variant carriers: 11

GenotypeDepth
all individuals: 1035
bin: 6.75e1
variant carriers: 17

GenotypeDepth
all individuals: 2396
bin: 5.75e1
variant carriers: 17

GenotypeDepth
all individuals: 291
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2007
bin: 9.75e1
variant carriers: 21

GenotypeDepth
all individuals: 258
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 354
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29031
bin: 9.75e1
variant carriers: 223

GenotypeQuality
all individuals: 2797
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2731
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 220
allele frequency: 2.116605734077352e-2
allele num: 10394
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

DP
type: SiteQuality
SIO_000300: 2.569926e6

MQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

MQ
type: SiteQuality
SIO_000300: 5.847e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.424e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.318+15G>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.318+15G>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7573
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5581
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2399
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 352
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10035
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8761
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6163
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9368
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1612
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3657
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28968
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3936
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

VQSLOD
type: SiteQuality
SIO_000300: -2.331e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.058e0

FS
type: SiteQuality
SIO_000300: 3.955e0

DP
type: SiteQuality
SIO_000300: 2.571315e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.042e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.258+13T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.399+13T>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5582
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6187
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9369
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10042
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7575
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8782
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3656
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8380
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4286
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3936
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28975
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4438
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

FS
type: SiteQuality
SIO_000300: 9.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.572001e6

MQ
type: SiteQuality
SIO_000300: 5.795e1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e0

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.392e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.494A>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450121
ensembl transcript: ENST00000547191
gene symbol: RPLP0
hgvsc: ENST00000547191.1:c.272A>G
hgvsp: ENSP00000450121.1:p.Asn91Ser
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.314A>G
hgvsp: ENSP00000449205.1:p.Asn105Ser
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.356A>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5583
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2399
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3658
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9388
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7583
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6187
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8864
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10152
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28991
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2758
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 5.897e1

DP
type: SiteQuality
SIO_000300: 2.575881e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.348G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.246G>C
hgvsp: ENSP00000449854.1:p.Leu82Phe
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*143G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.486G>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5584
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2400
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7597
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9402
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3659
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8902
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10187
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6122
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29001
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

DP
type: SiteQuality
SIO_000300: 2.577266e6

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -1.271e0

QD
type: SiteQuality
SIO_000300: 1.158e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 6.016e0

MQ
type: SiteQuality
SIO_000300: 5.717e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.287C>T
hgvsp: ENSP00000448639.1:p.Thr96Ile
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.593C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.467C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.227C>T
hgvsp: ENSP00000449854.1:p.Thr76Ile
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2401
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9408
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10233
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7601
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5584
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6054
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8943
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3659
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3948
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29005
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4515
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

QD
type: SiteQuality
SIO_000300: 1.475e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.566e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

DP
type: SiteQuality
SIO_000300: 2.578528e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.369C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*119C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1853C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.462C>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9407
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3659
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8955
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6032
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10239
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2401
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7601
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5584
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3950
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29006
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.186e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.52e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

VQSLOD
type: SiteQuality
SIO_000300: -2.815e-1

DP
type: SiteQuality
SIO_000300: 2.578707e6

MQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.363G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.276G>A
hgvsp: ENST00000551150.1:c.276G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.325G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.456G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 10109
bin: 3.25e1
variant carriers: 7

GenotypeDepth
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8823
bin: 2.75e1
variant carriers: 7

GenotypeDepth
all individuals: 5933
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9292
bin: 3.75e1
variant carriers: 13

GenotypeDepth
all individuals: 7531
bin: 4.25e1
variant carriers: 36

GenotypeDepth
all individuals: 3668
bin: 5.25e1
variant carriers: 57

GenotypeDepth
all individuals: 5551
bin: 4.75e1
variant carriers: 39

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 758
bin: 7.25e1
variant carriers: 76

GenotypeDepth
all individuals: 43
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1670
bin: 6.25e1
variant carriers: 73

GenotypeDepth
all individuals: 2135
bin: 9.75e1
variant carriers: 173

GenotypeDepth
all individuals: 581
bin: 7.75e1
variant carriers: 76

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1099
bin: 6.75e1
variant carriers: 81

GenotypeDepth
all individuals: 348
bin: 8.75e1
variant carriers: 53

GenotypeDepth
all individuals: 2429
bin: 5.75e1
variant carriers: 60

GenotypeDepth
all individuals: 287
bin: 9.25e1
variant carriers: 34

GenotypeDepth
all individuals: 412
bin: 8.25e1
variant carriers: 64

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4647
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3895
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29461
bin: 9.75e1
variant carriers: 850

GenotypeQuality
all individuals: 2884
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 18
allele frequency: 1.730103806228374e-3
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 30
allele frequency: 2.592912705272256e-3
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 41
allele frequency: 2.483042635658915e-3
allele num: 16512
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 748
allele frequency: 1.121069512304787e-2
allele num: 66722
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.023888720895071e-3
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

DP
type: SiteQuality
SIO_000300: 2.60952e6

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.348G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1838G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.354G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000447311
ensembl transcript: ENST00000546990
gene symbol: RPLP0
hgvsc: ENST00000546990.1:c.267G>A
hgvsp: ENST00000546990.1:c.267G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.207G>A
hgvsp: ENST00000547211.1:c.207G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 9345
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8846
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5611
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5904
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7582
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2470
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3703
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3926
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8208
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4281
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2745
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4477
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.155e0

QD
type: SiteQuality
SIO_000300: 5.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.054e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.054e0

DP
type: SiteQuality
SIO_000300: 2.594282e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.62e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.564G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.307G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*95G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1829G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.449G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5613
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9348
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10146
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3702
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8865
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5871
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7584
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8205
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3927
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.304e0

QD
type: SiteQuality
SIO_000300: 8.33e0

DP
type: SiteQuality
SIO_000300: 2.594559e6

MQ
type: SiteQuality
SIO_000300: 5.811e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.349e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.337G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.562G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.256G>A
hgvsp: ENSP00000450019.1:p.Val86Met
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.305G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.447G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 9349
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10146
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8862
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7583
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3702
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5874
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5613
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 730
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3928
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4480
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4291
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.881e1

VQSLOD
type: SiteQuality
SIO_000300: -6.719000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.521e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.508e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

DP
type: SiteQuality
SIO_000300: 2.59457e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.435T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.661T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.446T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*92T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.342T>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 2472
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7582
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10149
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9353
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8861
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5613
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3701
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5865
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3928
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.064e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 2.302e0

QD
type: SiteQuality
SIO_000300: 1.422e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.525e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.594594e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.440G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.655G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448223
ensembl transcript: ENST00000551914
gene symbol: RPLP0
hgvsc: ENST00000551914.1:c.249G>A
hgvsp: ENST00000551914.1:c.249G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.189G>A
hgvsp: ENST00000547211.1:c.189G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*86G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1081
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10156
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 730
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9358
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3704
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5830
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5615
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8872
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7586
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2472
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.402e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.308e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

QD
type: SiteQuality
SIO_000300: 1.032e1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

DP
type: SiteQuality
SIO_000300: 2.595187e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.553C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448046
ensembl transcript: ENST00000550856
gene symbol: RPLP0
hgvsc: ENST00000550856.1:c.247C>T
hgvsp: ENSP00000448046.1:p.Arg83Trp
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*84C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.296C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.427C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5619
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8867
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5820
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7585
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9360
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3705
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10168
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29341
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.421e1

FS
type: SiteQuality
SIO_000300: 2.214e0

DP
type: SiteQuality
SIO_000300: 2.595324e6

MQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

MQ
type: SiteQuality
SIO_000300: 5.845e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*80T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450121
ensembl transcript: ENST00000547191
gene symbol: RPLP0
hgvsc: ENST00000547191.1:c.201T>C
hgvsp: ENST00000547191.1:c.201T>C(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.285T>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.243T>C
hgvsp: ENST00000228306.4:c.243T>C(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.324T>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5619
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5812
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7587
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10167
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8865
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3705
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9361
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4677
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29344
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.595269e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 7.997e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.141e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.111e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.241C>T
hgvsp: ENSP00000376299.4:p.His81Tyr
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448223
ensembl transcript: ENST00000551914
gene symbol: RPLP0
hgvsc: ENST00000551914.1:c.241C>T
hgvsp: ENSP00000448223.1:p.His81Tyr
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000447311
ensembl transcript: ENST00000546990
gene symbol: RPLP0
hgvsc: ENST00000546990.1:c.241C>T
hgvsp: ENSP00000447311.1:p.His81Tyr
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.421C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.647C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8867
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5621
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10169
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7591
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5800
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9363
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3705
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3931
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29343
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.545e0

MQRankSum
type: SiteQuality
SIO_000300: -2.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

VQSLOD
type: SiteQuality
SIO_000300: -8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.997e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.595505e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.239C>T
hgvsp: ENSP00000376299.4:p.Pro80Leu
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.179C>T
hgvsp: ENSP00000449854.1:p.Pro60Leu
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.645C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1810C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.419C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5794
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3706
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5619
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7592
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9362
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10180
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8857
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8125
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2904
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.198e0

VQSLOD
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.857e0

DP
type: SiteQuality
SIO_000300: 2.595536e6

MQ
type: SiteQuality
SIO_000300: 5.885e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.237G>C
hgvsp: ENST00000546989.1:c.237G>C(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448223
ensembl transcript: ENST00000551914
gene symbol: RPLP0
hgvsc: ENST00000551914.1:c.237G>C
hgvsp: ENST00000551914.1:c.237G>C(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.324G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.237G>C
hgvsp: ENST00000547173.1:c.237G>C(p.%3D)
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 7593
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3706
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5620
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8853
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5772
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9364
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8035
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4303
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.192e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

FS
type: SiteQuality
SIO_000300: 3.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.297e0

DP
type: SiteQuality
SIO_000300: 2.595627e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448223
ensembl transcript: ENST00000551914
gene symbol: RPLP0
hgvsc: ENST00000551914.1:c.234G>A
hgvsp: ENST00000551914.1:c.234G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.234G>A
hgvsp: ENST00000551150.1:c.234G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.414G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.321G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.276G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8846
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3706
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5774
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10197
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5620
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7598
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9361
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3932
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 2.595762e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.441e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.179e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448046
ensembl transcript: ENST00000550856
gene symbol: RPLP0
hgvsc: ENST00000550856.1:c.231-5T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.231-5T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.273-5T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.189-5T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.632T>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10214
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9372
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2473
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8851
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5723
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7593
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3706
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5623
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29356
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3934
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4312
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997422216893472e-5
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.133e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

DP
type: SiteQuality
SIO_000300: 2.596169e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 1.596e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.280-10C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.231-10C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.189-10C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10221
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5623
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3707
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5702
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8843
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7597
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2474
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9373
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.59623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 8.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.444e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.42e-1

FS
type: SiteQuality
SIO_000300: 4.05e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.231-13C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.231-13C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.273-13C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 3709
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5688
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5623
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8854
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10220
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9377
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2473
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7597
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4318
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7947
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2754
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.114e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.317e0

DP
type: SiteQuality
SIO_000300: 2.596351e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

FS
type: SiteQuality
SIO_000300: 1.5243e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.31e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.537-20C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*68-20C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.312-20C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7605
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8851
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3710
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2475
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10243
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9383
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5638
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5628
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7912
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29362
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.407e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 2.753e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 2.596976e6

VQSLOD
type: SiteQuality
SIO_000300: -2.515e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.231-31G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.280-31G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.231-31G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 9403
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2474
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2014
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3710
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8831
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5628
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7609
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5623
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10244
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2924
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2765
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29373
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.597178e6

QD
type: SiteQuality
SIO_000300: 1.312e1

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.776e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.773e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.44e0

FS
type: SiteQuality
SIO_000300: 3.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.4e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.273-38C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.280-38C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.231-38C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 3711
bin: 5.25e1
variant carriers: 14

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 6

GenotypeDepth
all individuals: 5606
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7619
bin: 4.25e1
variant carriers: 18

GenotypeDepth
all individuals: 266
bin: 9.25e1
variant carriers: 5

GenotypeDepth
all individuals: 8801
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 10227
bin: 3.25e1
variant carriers: 9

GenotypeDepth
all individuals: 736
bin: 7.25e1
variant carriers: 12

GenotypeDepth
all individuals: 1697
bin: 6.25e1
variant carriers: 13

GenotypeDepth
all individuals: 9397
bin: 3.75e1
variant carriers: 9

GenotypeDepth
all individuals: 1093
bin: 6.75e1
variant carriers: 18

GenotypeDepth
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5634
bin: 4.75e1
variant carriers: 15

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2032
bin: 9.75e1
variant carriers: 32

GenotypeDepth
all individuals: 549
bin: 7.75e1
variant carriers: 6

GenotypeDepth
all individuals: 2479
bin: 5.75e1
variant carriers: 12

GenotypeDepth
all individuals: 388
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 29477
bin: 9.75e1
variant carriers: 183

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4663
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7829
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.049083995852057e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 177
allele frequency: 1.701923076923077e-2
allele num: 10400
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.957e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 1.471e1

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

DP
type: SiteQuality
SIO_000300: 2.601688e6

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.189-41G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*68-41G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.280-41G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1090
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2033
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8799
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5636
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9409
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7617
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10229
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2477
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5600
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3711
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4346
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7803
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29455
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.683e1

VQSLOD
type: SiteQuality
SIO_000300: -4.358e-1

FS
type: SiteQuality
SIO_000300: 3.578e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.601908e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.291e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.755e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.189-42G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.537-42G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.231-42G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2034
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1090
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5638
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8791
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7616
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10231
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5602
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1703
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2479
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9407
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3712
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29463
bin: 9.75e1
variant carriers: 11

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648483395276346e-4
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.588e0

FS
type: SiteQuality
SIO_000300: 5.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

DP
type: SiteQuality
SIO_000300: 2.602246e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.231-46G>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.273-46G>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.231-46G>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1701
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2479
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5616
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5638
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10222
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1093
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7620
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8792
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2034
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9407
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3712
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29471
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3959
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4660
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.579e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 2.602409e6

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.231-48G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448223
ensembl transcript: ENST00000551914
gene symbol: RPLP0
hgvsc: ENST00000551914.1:c.231-48G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.231-48G>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7615
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 10226
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5616
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 392
bin: 8.25e1
variant carriers: 4

GenotypeDepth
all individuals: 3712
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 8783
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5639
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2479
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2043
bin: 9.75e1
variant carriers: 13

GenotypeDepth
all individuals: 325
bin: 8.75e1
variant carriers: 3

GenotypeDepth
all individuals: 9404
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1095
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29486
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 4658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.444071454262079e-4
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 2.603971e6

QD
type: SiteQuality
SIO_000300: 1.566e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.231-51C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450121
ensembl transcript: ENST00000547191
gene symbol: RPLP0
hgvsc: ENST00000547191.1:c.189-51C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1802-51C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 5601
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5640
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10229
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2478
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3710
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7619
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8791
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9409
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2045
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1093
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3960
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29497
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.604397e6

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.23e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.317e0

QD
type: SiteQuality
SIO_000300: 1.406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*68-52C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.537-52C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.280-52C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 8796
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10230
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7618
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2477
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3711
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5644
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9405
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1094
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5596
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1706
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2046
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 551
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29505
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.942e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

QD
type: SiteQuality
SIO_000300: 1.342e1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

DP
type: SiteQuality
SIO_000300: 2.604696e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.324e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.272+50C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1801+50C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.188+50C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28794
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1528
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 653
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10120
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 895
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9818
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 687
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1037
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.992e0

VQSLOD
type: SiteQuality
SIO_000300: -1.667e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

FS
type: SiteQuality
SIO_000300: 1.8766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

DP
type: SiteQuality
SIO_000300: 2.147765e6

QD
type: SiteQuality
SIO_000300: 1.383e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.230+50C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448046
ensembl transcript: ENST00000550856
gene symbol: RPLP0
hgvsc: ENST00000550856.1:c.230+50C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.279+50C>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28794
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9818
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1528
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1037
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10120
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 895
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 580
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 653
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10075
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6780
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.667e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.992e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

FS
type: SiteQuality
SIO_000300: 1.8766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 2.147765e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.272+45T>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.311+45T>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.230+45T>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 682
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9808
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 578
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 970
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10132
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28803
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 896
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1524
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1065
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10071
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39606
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049003446725611e-4
allele num: 66730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.242e0

VQSLOD
type: SiteQuality
SIO_000300: 3.72e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.147257e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1801+44C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*67+44C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448046
ensembl transcript: ENST00000550856
gene symbol: RPLP0
hgvsc: ENST00000550856.1:c.230+44C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 644
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1063
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 578
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28804
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9802
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10141
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 895
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1751
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10064
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994305409860632e-5
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.576e1

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

DP
type: SiteQuality
SIO_000300: 2.146757e6

FS
type: SiteQuality
SIO_000300: 2.009e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.458e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.230+42G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*67+42G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450222
ensembl transcript: ENST00000547475
gene symbol: RPLP0
hgvsc: ENST00000547475.1:c.230+42G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 578
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 643
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9799
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28801
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1750
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 894
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6765
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10055
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

VQSLOD
type: SiteQuality
SIO_000300: -2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

FS
type: SiteQuality
SIO_000300: 1.633e1

DP
type: SiteQuality
SIO_000300: 2.146406e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

QD
type: SiteQuality
SIO_000300: 1.311e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000366471
ensembl transcript: ENST00000313104
gene symbol: RPLP0
hgvsc: ENST00000313104.5:c.230+41C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.230+41C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.272+41C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 575
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 677
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10161
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28806
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 644
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 652
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1752
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 9787
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 970
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 893
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10051
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.098069775806258e-4
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

DP
type: SiteQuality
SIO_000300: 2.146255e6

QD
type: SiteQuality
SIO_000300: 1.475e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.311+41C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.536+41C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.230+41C>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 10161
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9787
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1752
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28806
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 970
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 893
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 575
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 644
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 677
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10051
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 2.146255e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 1.475e1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.230+39C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.230+39C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.536+39C>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 674
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 827
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 892
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28810
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 575
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10186
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9779
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1746
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10041
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

QD
type: SiteQuality
SIO_000300: 1.454e1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 2.145226e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.377e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.044e0

FS
type: SiteQuality
SIO_000300: 3.76e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448046
ensembl transcript: ENST00000550856
gene symbol: RPLP0
hgvsc: ENST00000550856.1:c.230+34C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+34C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.536+34C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1748
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 891
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1510
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10227
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 641
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28801
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 576
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9763
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 722
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10033
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

DP
type: SiteQuality
SIO_000300: 2.144842e6

FS
type: SiteQuality
SIO_000300: 2.224e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.435e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.311+33C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.230+33C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.230+33C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 571
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28809
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10234
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 670
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1746
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1510
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 890
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9758
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10030
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39700
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.68787238131847e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.5e1

DP
type: SiteQuality
SIO_000300: 2.144644e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

FS
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.317+32C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+32C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.188+32C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1504
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 643
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9753
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 889
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10250
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1742
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28820
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 669
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10022
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39728
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.143731e6

QD
type: SiteQuality
SIO_000300: 1.579e1

FS
type: SiteQuality
SIO_000300: 1.935e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.355e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.279+29C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.230+29C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+29C>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10270
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28822
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1742
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 569
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9743
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 649
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 891
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1495
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 669
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1032
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 486
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10025
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.267441860465116e-4
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.905e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.143505e6

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

QD
type: SiteQuality
SIO_000300: 1.383e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+25C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.342C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.279+25C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 639
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 487
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 648
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9726
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1492
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10293
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 665
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 967
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1060
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28832
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1748
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10012
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.397650302703351e-4
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.143295e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.343e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.933e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.279+20T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+20T>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.317+20T>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 9719
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1740
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1059
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 966
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 639
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10307
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28852
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 663
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9996
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39817
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.14181e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 9.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.044e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449205
ensembl transcript: ENST00000546989
gene symbol: RPLP0
hgvsc: ENST00000546989.1:c.230+17G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.279+17G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1801+17G>C
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9718
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28849
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1739
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 663
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 966
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 888
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10309
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1058
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9994
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.347e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e0

VQSLOD
type: SiteQuality
SIO_000300: -1.441e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.898e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.141762e6

QD
type: SiteQuality
SIO_000300: 1.107e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.230+11C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*67+11C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.311+11C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 10342
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 641
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1477
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1058
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9708
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 656
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 967
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28854
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1739
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39877
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 2.141471e6

MQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.237e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.974e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.170+8C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450121
ensembl transcript: ENST00000547191
gene symbol: RPLP0
hgvsc: ENST00000547191.1:c.188+8C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.540C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448639
ensembl transcript: ENST00000551258
gene symbol: RPLP0
hgvsc: ENST00000551258.1:c.230+8C>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450222
ensembl transcript: ENST00000547475
gene symbol: RPLP0
hgvsc: ENST00000547475.1:c.230+8C>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9701
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1058
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 642
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1740
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10360
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28859
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1028
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1471
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6749
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9992
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.479e0

DP
type: SiteQuality
SIO_000300: 2.141363e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.596e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.15e0

FS
type: SiteQuality
SIO_000300: 1.5773e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1799G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: true
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.228G>A
hgvsp: ENST00000551150.1:c.228G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.304G>A
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449765
ensembl transcript: ENST00000550423
gene symbol: RPLP0
hgvsc: ENST00000550423.1:c.186G>A
hgvsp: ENST00000550423.1:c.186G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.168G>A
hgvsp: ENST00000547211.1:c.168G>A(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*65G>A
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 9693
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10373
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1465
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28874
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1028
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 566
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1058
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1739
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9988
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39950
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.201e1

VQSLOD
type: SiteQuality
SIO_000300: -1.732e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.754e0

DP
type: SiteQuality
SIO_000300: 2.141081e6

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 4.494e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.455e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.223C>T
hgvsp: ENST00000551150.1:c.223C>T(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.310C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.265C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.299C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.304C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10377
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1462
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9687
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28896
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 886
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1742
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9986
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

DP
type: SiteQuality
SIO_000300: 2.141293e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.65e-2

FS
type: SiteQuality
SIO_000300: 2.515e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

QD
type: SiteQuality
SIO_000300: 1.283e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.845e0

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449328
ensembl transcript: ENST00000551150
gene symbol: RPLP0
hgvsc: ENST00000551150.1:c.223C>G
hgvsp: ENSP00000449328.1:p.Leu75Val
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.299C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.525C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548495
gene symbol: RPLP0
hgvsc: ENST00000548495.1:n.310C>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.304C>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10377
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 886
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1462
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28896
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9687
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1742
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9986
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.845e0

FS
type: SiteQuality
SIO_000300: 2.515e0

MQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.65e-2

QD
type: SiteQuality
SIO_000300: 1.283e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.141293e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548568
gene symbol: RPLP0
hgvsc: ENST00000548568.1:n.265C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.518C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*53C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000447311
ensembl transcript: ENST00000546990
gene symbol: RPLP0
hgvsc: ENST00000546990.1:c.216C>T
hgvsp: ENST00000546990.1:c.216C>T(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1787C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1740
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10393
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28912
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9685
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9983
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

FS
type: SiteQuality
SIO_000300: 4.579e0

QD
type: SiteQuality
SIO_000300: 1.34e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

DP
type: SiteQuality
SIO_000300: 2.141218e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000548551
gene symbol: RPLP0
hgvsc: ENST00000548551.1:n.284G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000450019
ensembl transcript: ENST00000547173
gene symbol: RPLP0
hgvsc: ENST00000547173.1:c.197G>C
hgvsp: ENSP00000450019.1:p.Arg66Pro
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.499G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000549242
gene symbol: RPLP0
hgvsc: ENST00000549242.1:n.273G>C
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000449854
ensembl transcript: ENST00000547211
gene symbol: RPLP0
hgvsc: ENST00000547211.1:c.137G>C
hgvsp: ENSP00000449854.1:p.Arg46Pro
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28933
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 566
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9679
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10404
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 885
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1453
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9983
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 1.544e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.24e-1

DP
type: SiteQuality
SIO_000300: 2.141355e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e0

VQSLOD
type: SiteQuality
SIO_000300: -1.363e0

QD
type: SiteQuality
SIO_000300: 2.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.494C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000376299
ensembl transcript: ENST00000392514
gene symbol: RPLP0
hgvsc: ENST00000392514.4:c.192C>T
hgvsp: ENST00000392514.4:c.192C>T(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000447311
ensembl transcript: ENST00000546990
gene symbol: RPLP0
hgvsc: ENST00000546990.1:c.192C>T
hgvsp: ENST00000546990.1:c.192C>T(p.%3D)
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552902
gene symbol: RPLP0
hgvsc: ENST00000552902.1:n.498C>T
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000550296
gene symbol: RPLP0
hgvsc: ENST00000550296.1:n.234C>T
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 964
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 566
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1027
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9673
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28941
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10414
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 885
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1451
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1741
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9983
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

FS
type: SiteQuality
SIO_000300: 3.192e0

QD
type: SiteQuality
SIO_000300: 1.186e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.034e0

DP
type: SiteQuality
SIO_000300: 2.141328e6

MQ
type: SiteQuality
SIO_000300: 5.818e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.253e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.409e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000552461
gene symbol: RPLP0
hgvsc: ENST00000552461.1:n.1759A>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000546564
gene symbol: RPLP0
hgvsc: ENST00000546564.1:n.269A>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000089157
ensembl transcript: ENST00000551783
gene symbol: RPLP0
hgvsc: ENST00000551783.1:n.490A>G
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000339027
ensembl transcript: ENST00000228306
gene symbol: RPLP0
hgvsc: ENST00000228306.4:c.188A>G
hgvsp: ENSP00000339027.3:p.Lys63Arg
variant of: http://identifiers.org/hgnc/10371

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000089157
ensembl protein: ENSP00000448919
ensembl transcript: ENST00000549098
gene symbol: RPLP0
hgvsc: ENST00000549098.1:c.*25A>G
variant of: http://identifiers.org/hgnc/10371

GenotypeDepth
all individuals: 825
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 885
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28948
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1741
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1450
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10408
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9677
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1026
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0