X-153629132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629132
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629132
    reference: chr 0
allele count: 1
allele frequency: 1.229392311380485e-5
allele num: 81341
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+850C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1203C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1412C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1609C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.419C>T
  hgvsp: ENSP00000395025.1:p.Ala140Val
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.582C>T
  hgvsp: ENST00000424325.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.429C>T
  hgvsp: ENST00000406022.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.582C>T
  hgvsp: ENST00000369817.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.582C>T
  hgvsp: ENST00000344746.4:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.680C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+165C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+165C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000388600
  ensembl transcript: ENST00000436473
  gene symbol: RPL10
  hgvsc: ENST00000436473.1:c.582C>T
  hgvsp: ENST00000436473.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1247C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+850C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000485196
  gene symbol: RPL10
  hgvsc: ENST00000485196.1:n.813C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala140Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

X-153629132-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629132
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629132
    reference: chr 0
allele count: 1
allele frequency: 1.229392311380485e-5
allele num: 81341
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000485196
  gene symbol: RPL10
  hgvsc: ENST00000485196.1:n.813C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.582C>A
  hgvsp: ENST00000369817.2:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.419C>A
  hgvsp: ENSP00000395025.1:p.Ala140Asp
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.582C>A
  hgvsp: ENST00000344746.4:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000388600
  ensembl transcript: ENST00000436473
  gene symbol: RPL10
  hgvsc: ENST00000436473.1:c.582C>A
  hgvsp: ENST00000436473.1:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.429C>A
  hgvsp: ENST00000406022.2:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.582C>A
  hgvsp: ENST00000424325.2:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1412C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+165C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1247C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1203C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1609C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+850C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.680C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+850C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+165C>A
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala140Asp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-153629155-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629155
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629155
    reference: chr 0
allele count: 66976
allele frequency: 8.260789126386028e-1
allele num: 81077
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1270A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+873A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.605A>G
  hgvsp: ENSP00000341730.4:p.Asn202Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.605A>G
  hgvsp: ENSP00000413436.2:p.Asn202Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.442A>G
  hgvsp: ENSP00000395025.1:p.Ile148Val
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.452A>G
  hgvsp: ENSP00000385621.2:p.Asn151Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.703A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.605A>G
  hgvsp: ENSP00000358832.2:p.Asn202Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1435A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1226A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+873A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+188A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000485196
  gene symbol: RPL10
  hgvsc: ENST00000485196.1:n.836A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+188A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1632A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.75e1
  variant carriers: 1485
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 1.75e1
  variant carriers: 9532
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 7.5e0
  variant carriers: 2824
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 895
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 2.25e1
  variant carriers: 7244
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 3.75e1
  variant carriers: 3639
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 4.25e1
  variant carriers: 2261
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 3.25e1
  variant carriers: 4787
genotype quality: GenotypeQuality
hgvs: p.Asn202Ser
num of homozygotes: 17974
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

X-153629157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629157
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629157
    reference: chr 0
allele count: 1
allele frequency: 1.349782684987717e-5
allele num: 74086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.607C>T
  hgvsp: ENSP00000358832.2:p.Arg203Cys
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1228C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+875C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.454C>T
  hgvsp: ENSP00000385621.2:p.Arg152Cys
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+190C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.607C>T
  hgvsp: ENSP00000413436.2:p.Arg203Cys
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.444C>T
  hgvsp: ENST00000458500.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000485196
  gene symbol: RPL10
  hgvsc: ENST00000485196.1:n.838C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1437C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+190C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.607C>T
  hgvsp: ENSP00000341730.4:p.Arg203Cys
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1272C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1634C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+875C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.705C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg203Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

X-153629158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629158
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629158
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 73787
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.608G>A
  hgvsp: ENSP00000413436.2:p.Arg203His
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.608G>A
  hgvsp: ENSP00000341730.4:p.Arg203His
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.608G>A
  hgvsp: ENSP00000358832.2:p.Arg203His
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000485196
  gene symbol: RPL10
  hgvsc: ENST00000485196.1:n.839G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1438G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+876G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.445G>A
  hgvsp: ENSP00000395025.1:p.Val149Met
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+876G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1229G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.706G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+191G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1635G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.455G>A
  hgvsp: ENSP00000385621.2:p.Arg152His
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1273G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+191G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg203His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

X-153629166-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629166
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629166
    reference: chr 0
allele count: 1
allele frequency: 1.376140476419833e-5
allele num: 72667
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+199C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+199C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1446C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.616C>A
  hgvsp: ENSP00000341730.4:p.Leu206Met
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.463C>A
  hgvsp: ENSP00000385621.2:p.Leu155Met
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.714C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.616C>A
  hgvsp: ENSP00000358832.2:p.Leu206Met
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1281C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1237C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+884C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.453C>A
  hgvsp: ENST00000458500.1:c.453C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.616C>A
  hgvsp: ENSP00000413436.2:p.Leu206Met
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+884C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1643C>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu206Met
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

X-153629168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629168
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629168
    reference: chr 0
allele count: 1
allele frequency: 1.384274640088594e-5
allele num: 72240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+201G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.716G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1645G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.618G>A
  hgvsp: ENST00000344746.4:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.618G>A
  hgvsp: ENST00000369817.2:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1283G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.465G>A
  hgvsp: ENST00000406022.2:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.455G>A
  hgvsp: ENSP00000395025.1:p.Trp152Ter
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.618G>A
  hgvsp: ENST00000424325.2:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+886G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+201G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1239G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1448G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+886G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp152Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-153629179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629179
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629179
    reference: chr 0
allele count: 13
allele frequency: 1.963301366759798e-4
allele num: 66215
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1250G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+212G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+212G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.629G>A
  hgvsp: ENSP00000341730.4:p.Arg210Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1656G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.476G>A
  hgvsp: ENSP00000385621.2:p.Arg159Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.629G>A
  hgvsp: ENSP00000358832.2:p.Arg210Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+897G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1294G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.727G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+897G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.629G>A
  hgvsp: ENSP00000413436.2:p.Arg210Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.466G>A
  hgvsp: ENSP00000395025.1:p.Gly156Arg
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1459G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8392
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg210Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-153629180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629180
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629180
    reference: chr 0
allele count: 7
allele frequency: 1.057593521484257e-4
allele num: 66188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+213G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+213G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1460G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+898G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.467G>A
  hgvsp: ENSP00000395025.1:p.Gly156Glu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.630G>A
  hgvsp: ENST00000369817.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1251G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1657G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.630G>A
  hgvsp: ENST00000344746.4:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+898G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.477G>A
  hgvsp: ENST00000406022.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.728G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.630G>A
  hgvsp: ENST00000424325.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1295G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12799
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly156Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

X-153629183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629183
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629183
    reference: chr 0
allele count: 140
allele frequency: 2.146580803434529e-3
allele num: 65220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1254C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.480C>T
  hgvsp: ENST00000406022.2:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1660C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+216C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.470C>T
  hgvsp: ENSP00000395025.1:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+901C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.731C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1463C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.633C>T
  hgvsp: ENST00000344746.4:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.633C>T
  hgvsp: ENST00000369817.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1298C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+901C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+216C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.633C>T
  hgvsp: ENST00000424325.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15913
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 9265
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Pro157Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

X-153629189-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629189
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629189
    reference: chr 0
allele count: 2
allele frequency: 3.115458907097015e-5
allele num: 64196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+907C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.639C>G
  hgvsp: ENSP00000358832.2:p.His213Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1666C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.737C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1304C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.486C>G
  hgvsp: ENSP00000385621.2:p.His162Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.639C>G
  hgvsp: ENSP00000413436.2:p.His213Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+907C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.639C>G
  hgvsp: ENSP00000341730.4:p.His213Gln
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+222C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+222C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1469C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1260C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.476C>G
  hgvsp: ENSP00000395025.1:p.Thr159Ser
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His213Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

X-153629191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629191
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629191
    reference: chr 0
allele count: 3
allele frequency: 4.671296440472112e-5
allele num: 64222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1668C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1306C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+224C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1262C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.641C>T
  hgvsp: ENSP00000413436.2:p.Ser214Leu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.488C>T
  hgvsp: ENSP00000385621.2:p.Ser163Leu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.739C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1471C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+909C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.641C>T
  hgvsp: ENSP00000341730.4:p.Ser214Leu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.478C>T
  hgvsp: ENSP00000395025.1:p.His160Tyr
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+224C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.641C>T
  hgvsp: ENSP00000358832.2:p.Ser214Leu
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+909C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser214Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS

X-153629197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629197
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629197
    reference: chr 0
allele count: 1
allele frequency: 1.567275291905023e-5
allele num: 63805
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1312G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.745G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*2G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1674G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+915G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1477G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*2G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.484G>A
  hgvsp: ENSP00000395025.1:p.Gly162Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*2G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+230G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+230G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+915G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1268G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*2G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly162Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-153629197-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629197
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629197
    reference: chr 0
allele count: 1
allele frequency: 1.567275291905023e-5
allele num: 63805
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1268G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*2G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+915G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*2G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+230G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1312G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1477G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*2G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*2G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.745G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+230G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1674G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+915G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.484G>C
  hgvsp: ENSP00000395025.1:p.Gly162Arg
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly162Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS

X-153629212-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629212
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629212
    reference: chr 0
allele count: 1
allele frequency: 1.59877214299418e-5
allele num: 62548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1283G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*17G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+930G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*17G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.760G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+245G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1492G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1689G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*17G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*17G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.499G>T
  hgvsp: ENSP00000395025.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+930G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+245G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1327G>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9855
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala167Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

X-153629214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629214
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629214
    reference: chr 0
allele count: 1
allele frequency: 1.601742696053306e-5
allele num: 62432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+247C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*19C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1285C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+247C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*19C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1494C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*19C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1329C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.501C>T
  hgvsp: ENST00000458500.1:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+932C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.762C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*19C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1691C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+932C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala167Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-153629215-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629215
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629215
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 62433
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1495C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+248C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.502C>G
  hgvsp: ENSP00000395025.1:p.Pro168Ala
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*20C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*20C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+933C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+933C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*20C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1286C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1330C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.763C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1692C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*20C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+248C>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro168Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-153629217-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629217
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629217
    reference: chr 0
allele count: 1
allele frequency: 1.609398889514766e-5
allele num: 62135
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*22C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.504C>A
  hgvsp: ENST00000458500.1:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*22C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+935C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1497C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*22C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.765C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+250C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*22C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1288C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+935C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1332C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1694C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+250C>A
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18314
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro168Pro
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

X-153629218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629218
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629218
    reference: chr 0
allele count: 2
allele frequency: 3.22742016169375e-5
allele num: 61969
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1498C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+251C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*23C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1695C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*23C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*23C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+936C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.766C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+936C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*23C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1289C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.505C>T
  hgvsp: ENSP00000395025.1:p.Leu169Phe
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1333C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+251C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14610
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu169Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

X-153629223-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629223
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629223
    reference: chr 0
allele count: 1
allele frequency: 1.63036389722186e-5
allele num: 61336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+941A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1338A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*28A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*28A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.771A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.510A>G
  hgvsp: ENST00000458500.1:c.510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1294A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*28A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+256A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*28A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1700A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+256A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1503A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+941A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu170Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS

X-153629227-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629227
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629227
    reference: chr 0
allele count: 1
allele frequency: 1.629540306679486e-5
allele num: 61367
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.514C>G
  hgvsp: ENSP00000395025.1:p.Leu172Val
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*32C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1298C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1704C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+945C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+260C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*32C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1342C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*32C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*32C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+260C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+945C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1507C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.775C>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu172Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-153629234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629234
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629234
    reference: chr 0
allele count: 1
allele frequency: 1.650410126916539e-5
allele num: 60591
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000492572
  gene symbol: RPL10
  hgvsc: ENST00000492572.1:n.1305A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000489200
  gene symbol: RPL10
  hgvsc: ENST00000489200.1:n.1514A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+267A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*39A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.782A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+952A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.521A>G
  hgvsp: ENSP00000395025.1:p.Asn174Ser
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*39A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1711A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+267A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1349A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*39A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*39A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+952A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn174Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-153629241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629241
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629241
    reference: chr 0
allele count: 4
allele frequency: 6.679357445813713e-5
allele num: 59886
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.789C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*46C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1356C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.528C>T
  hgvsp: ENST00000458500.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+959C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+959C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+274C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+274C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14699
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe176Phe
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

X-153629243-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629243
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629243
    reference: chr 0
allele count: 1
allele frequency: 1.678471919164792e-5
allele num: 59578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1720A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*48A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*48A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.530A>G
  hgvsp: ENSP00000395025.1:p.Tyr177Cys
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+276A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1358A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+276A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+961A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*48A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.791A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*48A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+961A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr177Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-153629244-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629244
    reference: chr 0
allele count: 4
allele frequency: 6.743884140070474e-5
allele num: 59313
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1359C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*49C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+277C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1721C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+962C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.792C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*49C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*49C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.531C>G
  hgvsp: ENSP00000395025.1:p.Tyr177Ter
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+962C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+277C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*49C>G
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr177Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

X-153629247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629247
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629247
    reference: chr 0
allele count: 1
allele frequency: 1.709869365980439e-5
allele num: 58484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+280C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+965C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+965C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.534C>T
  hgvsp: ENST00000458500.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*52C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1362C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1724C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+280C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.795C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe178Phe
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

X-153629248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629248
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629248
    reference: chr 0
allele count: 42
allele frequency: 7.18562874251497e-4
allele num: 58450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000482732
  gene symbol: RPL10
  hgvsc: ENST00000482732.1:n.1725C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000467168
  gene symbol: RPL10
  hgvsc: ENST00000467168.1:n.796C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+966C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.535C>T
  hgvsp: ENST00000458500.1:c.535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000385621
  ensembl transcript: ENST00000406022
  gene symbol: RPL10
  hgvsc: ENST00000406022.2:c.*53C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+281C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147403
  ensembl transcript: ENST00000491035
  gene symbol: RPL10
  hgvsc: ENST00000491035.1:n.1363C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*53C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+281C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*53C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*53C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+966C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10224
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13169
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19828
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9461
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: p.Leu179Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

X-153629256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629256
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629256
    reference: chr 0
allele count: 1
allele frequency: 1.836682217242773e-5
allele num: 54446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+974C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000395025
  ensembl transcript: ENST00000458500
  gene symbol: RPL10
  hgvsc: ENST00000458500.1:c.543C>T
  hgvsp: ENST00000458500.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*61C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+974C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+289C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*61C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+289C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000358832
  ensembl transcript: ENST00000369817
  gene symbol: RPL10
  hgvsc: ENST00000369817.2:c.*61C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr181Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-153629260-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629260
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629260
    reference: chr 0
allele count: 1
allele frequency: 1.904761904761905e-5
allele num: 52500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+978G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*65G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+293G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+293G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*65G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+978G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21029
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5653
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

X-153629268-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629268
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629268
    reference: chr 0
allele count: 1
allele frequency: 2.099340806986606e-5
allele num: 47634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+301A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+986A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+986A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*73A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+301A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*73A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8385
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-153629274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629274
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629274
    reference: chr 0
allele count: 1
allele frequency: 2.345986017923333e-5
allele num: 42626
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+992A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*79A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*79A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+307A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+307A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+992A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11646
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

X-153629274-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629274
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629274
    reference: chr 0
allele count: 1
allele frequency: 2.345986017923333e-5
allele num: 42626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+992A>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+307A>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*79A>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+992A>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+307A>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*79A>C
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11646
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29999
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-153629282-C-CCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629284
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 36992
alternate allele: CCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1000_59+1001insCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+315_222+316insCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*87_*88insCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*87_*88insCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1000_278+1001insCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+315_222+316insCA
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20646
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 15533
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-153629282-C-CCAGCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629287
    reference: chr 0
allele count: 1
allele frequency: 2.703287197231834e-5
allele num: 36992
alternate allele: CCAGCA
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*87_*88insCAGCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1000_278+1001insCAGCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+315_222+316insCAGCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1000_59+1001insCAGCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*87_*88insCAGCA
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+315_222+316insCAGCA
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15533
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-153629282-C-CCAGCAGCGTTTATTTAGCAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629302
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 36992
alternate allele: CCAGCAGCGTTTATTTAGCAA
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20646
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15533
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-153629282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629282
    reference: chr 0
allele count: 1
allele frequency: 2.703287197231834e-5
allele num: 36992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*87C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+315C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1000C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1000C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+315C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*87C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20646
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27374
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

X-153629283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629283
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629283
    reference: chr 0
allele count: 9
allele frequency: 2.486393900046965e-4
allele num: 36197
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+316G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1001G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1001G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+316G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*88G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*88G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11920
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16027
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-153629283-G-GCAGCGTTTATTTAGCAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629283
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629300
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 36197
alternate allele: GCAGCGTTTATTTAGCAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20555
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16027
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-153629285-G-GTAGGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629285
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629290
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 35194
alternate allele: GTAGGT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*90_*91insTAGGT
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*90_*91insTAGGT
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1003_59+1004insTAGGT
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+318_222+319insTAGGT
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+318_222+319insTAGGT
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1003_278+1004insTAGGT
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20314
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16955
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

X-153629287-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629287
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629287
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 34117
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+320A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*92A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+320A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1005A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1005A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*92A>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-153629294-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629294
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629294
    reference: chr 0
allele count: 170
allele frequency: 5.752571737953438e-3
allele num: 29552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*99T>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+327T>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1012T>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+327T>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*99T>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1012T>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 276
  bin: 7.25e1
  variant carriers: 3
num of homozygotes: 6
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-153629296-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629296
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629296
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 26277
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*101C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+329C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1014C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*101C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1014C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+329C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

X-153629297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629297
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629297
    reference: chr 0
allele count: 1
allele frequency: 3.811701924909472e-5
allele num: 26235
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+330C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*102C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*102C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1015C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+330C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1015C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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genotype depth: GenotypeDepth
  all individuals: 1331
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genotype depth: GenotypeDepth
  all individuals: 13
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genotype depth: GenotypeDepth
  all individuals: 158
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genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 290
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 32
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genotype depth: GenotypeDepth
  all individuals: 12
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
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genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 264
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genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

X-153629315-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629315
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629315
    reference: chr 0
allele count: 1
allele frequency: 5.997361161089121e-5
allele num: 16674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1033C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+348C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*120C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1033C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*120C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+348C>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 52
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12858
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  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

X-153629316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629316
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629316
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 16244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*121A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+349A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*121A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+349A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1034A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1034A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

X-153629325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629325
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629325
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 13107
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*130T>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+358T>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+358T>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*130T>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1043T>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1043T>C
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-153629328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629328
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629328
    reference: chr 0
allele count: 1
allele frequency: 8.169934640522875e-5
allele num: 12240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*133C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*133C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+361C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1046C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+361C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1046C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

X-153629331-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629331
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 11579
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1049C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+364C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1049C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+364C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*136C>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*136C>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

X-153629338-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629338
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629338
    reference: chr 0
allele count: 1
allele frequency: 9.716284492809949e-5
allele num: 10292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*143A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1056A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+371A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*143A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1056A>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+371A>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

X-153629347-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629347
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629347
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 8947
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*152A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+380A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1065A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
  ensembl transcript: ENST00000424325
  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*152A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1065A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+380A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-153629358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629358
    reference: chr 0
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    type: ExactPosition
    position: 24153629358
    reference: chr 0
allele count: 2
allele frequency: 2.641310089804543e-4
allele num: 7572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
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  ensembl protein: ENSP00000341730
  ensembl transcript: ENST00000344746
  gene symbol: RPL10
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
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  ensembl protein: ENSP00000406125
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  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1076C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
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  ensembl protein: ENSP00000413436
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000147403
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  gene symbol: RPL10
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  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

X-153629360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629360
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629360
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 7133
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1078C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1078C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000413436
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  gene symbol: RPL10
  hgvsc: ENST00000424325.2:c.*165C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  consequence: intron_variant
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*165C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
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site quality: MQRankSum
site quality: ClippingRankSum
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site quality: MQ
site quality: FS
site quality: DP
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site quality: QD

X-153629376-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629376
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629376
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 5713
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.59+1094C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
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  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.222+409C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  consequence: 3_prime_UTR_variant
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  gene symbol: RPL10
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  ensembl protein: ENSP00000398047
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  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+409C>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

X-153629378-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153629378
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153629378
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 5715
alternate allele: T
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000341730
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  gene symbol: RPL10
  hgvsc: ENST00000344746.4:c.*183G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
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  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.278+1096G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/10298
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  variant of: http://identifiers.org/hgnc/10298
canonical: true
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  variant carriers: 0
genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Other
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population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

X-153631017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631017
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631017
    reference: chr 0
allele count: 3
allele frequency: 8.168377487951644e-5
allele num: 36727
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2050G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-587G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-252G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.703C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*31C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-587G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

X-153631020-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631020
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631020
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 37672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2053A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.700T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-584A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*28T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-249A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-584A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28053
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4143
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

X-153631026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631026
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631026
    reference: chr 0
allele count: 1
allele frequency: 2.508843673950676e-5
allele num: 39859
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-578C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-243C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-578C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.694G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*22G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2059C>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

X-153631029-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631029
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631030
    reference: chr 0
allele count: 9
allele frequency: 2.2002200220022e-4
allele num: 40905
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-568dupG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.690dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-233dupG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2069dupG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*18dupC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-568dupG
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28345
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9225
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

X-153631030-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631030
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631030
    reference: chr 0
allele count: 35
allele frequency: 8.423180592991914e-4
allele num: 41552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-574G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2063G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.690C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*18C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-574G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-239G>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28297
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8605
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

X-153631031-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631031
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631031
    reference: chr 0
allele count: 1
allele frequency: 2.339017144995673e-5
allele num: 42753
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2064G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.689C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-573G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*17C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-238G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-573G>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-153631033-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631033
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631033
    reference: chr 0
allele count: 405
allele frequency: 9.033927416296758e-3
allele num: 44831
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-571G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2066G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.687C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*15C>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-571G>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-236G>T
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 1.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10597
  bin: 2.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 27996
  bin: 7.5e0
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.5e0
  variant carriers: 5
num of homozygotes: 11
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-153631036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631036
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631036
    reference: chr 0
allele count: 5
allele frequency: 1.081525383400748e-4
allele num: 46231
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-568G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.684C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-233G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*12C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-568G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2069G>A
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

X-153631039-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631039
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631039
    reference: chr 0
allele count: 1
allele frequency: 2.033594989221947e-5
allele num: 49174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-230G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2072G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.681C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*9C>G
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-565G>C
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-565G>C
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

X-153631041-G-GGGAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631041
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631045
    reference: chr 0
allele count: 1
allele frequency: 1.972970306796883e-5
allele num: 50685
alternate allele: GGGAC
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-561_223-558dupGACG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-561_279-558dupGACG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.675_678dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2076_222+2079dupGACG
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*3_*6dupGTCC
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-226_60-223dupGACG
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

X-153631045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631045
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631045
    reference: chr 0
allele count: 517
allele frequency: 9.720054898569253e-3
allele num: 53189
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.675G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-559C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-559C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-224C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2078C>T
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/2957
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 14897
  bin: 2.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24974
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 1.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 2.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 13
num of homozygotes: 10
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

X-153631046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631046
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631046
    reference: chr 0
allele count: 2
allele frequency: 3.672689878066696e-5
allele num: 54456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-558G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.674C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2079G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-558G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-223G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/2957
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

X-153631061-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631061
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631061
    reference: chr 0
allele count: 1
allele frequency: 1.562280304332203e-5
allele num: 64009
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-543C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.896G>C
  hgvsp: ENSP00000358824.1:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.896G>C
  hgvsp: ENSP00000358822.1:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.896G>C
  hgvsp: ENSP00000377255.1:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-208C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-543C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.659G>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.896G>C
  hgvsp: ENSP00000358823.3:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2094C>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.896G>C
  hgvsp: ENSP00000309168.5:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.896G>C
  hgvsp: ENSP00000014935.3:p.Cys299Ser
  variant of: http://identifiers.org/hgnc/2957
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys299Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-153631068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631068
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631068
    reference: chr 0
allele count: 1
allele frequency: 1.484670774255809e-5
allele num: 67355
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-201G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.889C>T
  hgvsp: ENSP00000358823.3:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000395591
  ensembl transcript: ENST00000447892
  gene symbol: DNASE1L1
  hgvsc: ENST00000447892.1:c.250C>T
  hgvsp: ENSP00000395591.1:p.Gln84Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.889C>T
  hgvsp: ENSP00000358824.1:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.889C>T
  hgvsp: ENSP00000358822.1:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.652C>T
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-536G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.889C>T
  hgvsp: ENSP00000377255.1:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.889C>T
  hgvsp: ENSP00000309168.5:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2101G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-536G>A
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.889C>T
  hgvsp: ENSP00000014935.3:p.Gln297Ter
  variant of: http://identifiers.org/hgnc/2957
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln297Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

X-153631074-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153631074
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153631074
    reference: chr 0
allele count: 1
allele frequency: 1.44005068978428e-5
allele num: 69442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000406125
  ensembl transcript: ENST00000451365
  gene symbol: RPL10
  hgvsc: ENST00000451365.1:c.279-530A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000013563
  ensembl transcript: ENST00000497242
  gene symbol: DNASE1L1
  hgvsc: ENST00000497242.1:n.646T>C
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000014935
  ensembl transcript: ENST00000014935
  gene symbol: DNASE1L1
  hgvsc: ENST00000014935.3:c.883T>C
  hgvsp: ENSP00000014935.3:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000395591
  ensembl transcript: ENST00000447892
  gene symbol: DNASE1L1
  hgvsc: ENST00000447892.1:c.244T>C
  hgvsp: ENSP00000395591.1:p.Ser82Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000309168
  ensembl transcript: ENST00000309585
  gene symbol: DNASE1L1
  hgvsc: ENST00000309585.5:c.883T>C
  hgvsp: ENSP00000309168.5:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000398047
  ensembl transcript: ENST00000428169
  gene symbol: RPL10
  hgvsc: ENST00000428169.1:c.222+2107A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000405064
  ensembl transcript: ENST00000427682
  gene symbol: RPL10
  hgvsc: ENST00000427682.1:c.223-530A>G
  variant of: http://identifiers.org/hgnc/10298
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000377255
  ensembl transcript: ENST00000393638
  gene symbol: DNASE1L1
  hgvsc: ENST00000393638.1:c.883T>C
  hgvsp: ENSP00000377255.1:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358822
  ensembl transcript: ENST00000369807
  gene symbol: DNASE1L1
  hgvsc: ENST00000369807.1:c.883T>C
  hgvsp: ENSP00000358822.1:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358823
  ensembl transcript: ENST00000369808
  gene symbol: DNASE1L1
  hgvsc: ENST00000369808.3:c.883T>C
  hgvsp: ENSP00000358823.3:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000013563
  ensembl protein: ENSP00000358824
  ensembl transcript: ENST00000369809
  gene symbol: DNASE1L1
  hgvsc: ENST00000369809.1:c.883T>C
  hgvsp: ENSP00000358824.1:p.Ser295Pro
  variant of: http://identifiers.org/hgnc/2957
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147403
  ensembl protein: ENSP00000407754
  ensembl transcript: ENST00000449494
  gene symbol: RPL10
  hgvsc: ENST00000449494.1:c.60-195A>G
  variant of: http://identifiers.org/hgnc/10298
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser295Pro
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 556
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5955
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12575
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9461
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3481
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.256012272706763e-5
allele num: 44326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4293
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9459
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

QD
type: SiteQuality
SIO_000300: 1.888e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

FS
type: SiteQuality
SIO_000300: 6.057e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.601e0

VQSLOD
type: SiteQuality
SIO_000300: -3.794e0

MQ
type: SiteQuality
SIO_000300: 3.181e1

DP
type: SiteQuality
SIO_000300: 1.346594e6

GenotypeDepth
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3137
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 824
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8532
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9950
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4882
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9461
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1303
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8886
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.600512163892446e-4
allele num: 6248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4293
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9459
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.601e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 3.181e1

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

FS
type: SiteQuality
SIO_000300: 6.057e0

VQSLOD
type: SiteQuality
SIO_000300: -3.794e0

DP
type: SiteQuality
SIO_000300: 1.346594e6

QD
type: SiteQuality
SIO_000300: 1.888e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

GenotypeDepth
all individuals: 9732
bin: 1.25e1
variant carriers: 7994

GenotypeDepth
all individuals: 782
bin: 6.25e1
variant carriers: 781

GenotypeDepth
all individuals: 1723
bin: 9.75e1
variant carriers: 1723

GenotypeDepth
all individuals: 635
bin: 6.75e1
variant carriers: 635

GenotypeDepth
all individuals: 1098
bin: 5.25e1
variant carriers: 1093

GenotypeDepth
all individuals: 485
bin: 7.25e1
variant carriers: 485

GenotypeDepth
all individuals: 7192
bin: 2.75e1
variant carriers: 5814

GenotypeDepth
all individuals: 316
bin: 8.25e1
variant carriers: 316

GenotypeDepth
all individuals: 373
bin: 7.75e1
variant carriers: 371

GenotypeQuality
all individuals: 460
bin: 2.5e0
variant carriers: 127

GenotypeQuality
all individuals: 3536
bin: 3.75e1
variant carriers: 3353

GenotypeQuality
all individuals: 596
bin: 7.5e0
variant carriers: 245

GenotypeQuality
all individuals: 3705
bin: 5.25e1
variant carriers: 3597

GenotypeQuality
all individuals: 3775
bin: 4.75e1
variant carriers: 3689

GenotypeQuality
all individuals: 3014
bin: 3.25e1
variant carriers: 2668

GenotypeQuality
all individuals: 1482
bin: 2.75e1
variant carriers: 1043

GenotypeQuality
all individuals: 1530
bin: 9.25e1
variant carriers: 1526

GenotypeQuality
all individuals: 854
bin: 1.75e1
variant carriers: 719

GenotypeQuality
all individuals: 3787
bin: 2.25e1
variant carriers: 1370

GenotypeQuality
all individuals: 2809
bin: 6.75e1
variant carriers: 2422

GenotypeQuality
all individuals: 19362
bin: 9.75e1
variant carriers: 19326

GenotypeQuality
all individuals: 1690
bin: 5.75e1
variant carriers: 1644

GenotypeQuality
all individuals: 419
bin: 1.25e1
variant carriers: 314

GenotypeQuality
all individuals: 5540
bin: 6.25e1
variant carriers: 2835

GenotypeQuality
all individuals: 2060
bin: 7.75e1
variant carriers: 1993

GenotypeQuality
all individuals: 896
bin: 8.75e1
variant carriers: 885

GenotypeQuality
all individuals: 1843
bin: 8.25e1
variant carriers: 1815

GenotypeQuality
all individuals: 1243
bin: 7.25e1
variant carriers: 1147

GenotypeQuality
all individuals: 1949
bin: 4.25e1
variant carriers: 1879

European (Finnish)
type: Population
allele count: 3721
allele frequency: 8.700023380874444e-1
allele num: 4277
num of homozygotes: 913

European (Non-Finnish)
type: Population
allele count: 40190
allele frequency: 9.048541066282421e-1
allele num: 44416
num of homozygotes: 11413

African
type: Population
allele count: 1677
allele frequency: 2.342833193629505e-1
allele num: 7158
num of homozygotes: 162

Latino
type: Population
allele count: 6914
allele frequency: 7.921631530705775e-1
allele num: 8728
num of homozygotes: 2115

Other
type: Population
allele count: 517
allele frequency: 8.659966499162479e-1
allele num: 597
num of homozygotes: 132

East Asian
type: Population
allele count: 5862
allele frequency: 9.291488349976225e-1
allele num: 6309
num of homozygotes: 1954

South Asian
type: Population
allele count: 8095
allele frequency: 8.43932443703086e-1
allele num: 9592
num of homozygotes: 1285

MQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQ
type: SiteQuality
SIO_000300: 3.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3124e2

DP
type: SiteQuality
SIO_000300: 1.736138e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.137e1

GenotypeDepth
all individuals: 4625
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17397
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2861
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3957
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6901
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.19717466778403e-4
allele num: 8353
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5919
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.092e1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.049e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.616e1

DP
type: SiteQuality
SIO_000300: 1.184396e6

GenotypeDepth
all individuals: 10521
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1184
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13980
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12471
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17650
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 816
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21214
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3937
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 545
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8331
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8800
num of homozygotes: 0

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

DP
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VQSLOD
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QD
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InbreedingCoeff
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FS
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8718
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.585983966899405e-5
allele num: 38670
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQ
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QD
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 6708
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3859
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8229
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.603895427559629e-5
allele num: 38404
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -6.1e-3

ClippingRankSum
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MQ
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FS
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: -1.317e0

VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6193
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3467
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34335
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.551127550411645e-3
allele num: 8381
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 3.138e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

QD
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SIO_000300: 2.68e1

MQRankSum
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SIO_000300: 5.74e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 2.7e-3

VQSLOD
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SIO_000300: -3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

DP
type: SiteQuality
SIO_000300: 1.008365e6

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 2.038735983690112e-4
allele num: 34335
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 7773
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5553
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 1

African
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num of homozygotes: 0

South Asian
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allele frequency: 1.624157844080847e-2
allele num: 8312
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.966566792251328e-5
allele num: 33709
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 6.047228857376107e-5
allele num: 33073
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

African
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Other
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South Asian
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 9.061801486135444e-5
allele num: 33106
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7613
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Finnish)
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South Asian
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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QD
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 32085
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African
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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VQSLOD
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QD
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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Other
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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Latino
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.137254901960784e-5
allele num: 31875
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

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

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

BaseQRankSum
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FS
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VQSLOD
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SIO_000300: -3.148e0

DP
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InbreedingCoeff
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SIO_000300: -8.200000000000001e-3

ClippingRankSum
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SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 3.706e1

ReadPosRankSum
type: SiteQuality
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.147128245476003e-5
allele num: 31775
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.88465887674331e-4
allele num: 5306
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3317
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: -2.86e-1

ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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SIO_000300: -6.9e-3

BaseQRankSum
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SIO_000300: -1.711e0

QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3303
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 7384
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 31404
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

African
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num of homozygotes: 0

East Asian
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allele frequency: 1.899335232668566e-4
allele num: 5265
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.39e-1

InbreedingCoeff
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DP
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SIO_000300: 9.78717e5

MQ
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SIO_000300: 3.912e1

FS
type: SiteQuality
SIO_000300: 3.222e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31426
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3304
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

East Asian
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allele count: 1
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allele num: 5265
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.109e1

QD
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DP
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SIO_000300: 9.82849e5

BaseQRankSum
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FS
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VQSLOD
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SIO_000300: -2.701e0

MQRankSum
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SIO_000300: 1.15e0

ClippingRankSum
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SIO_000300: 2.13e-1

ReadPosRankSum
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SIO_000300: 2.44e0

InbreedingCoeff
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SIO_000300: -7.4e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.928268414963363e-4
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.308943355476292e-4
allele num: 30559
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FS
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 1.322576378785875e-4
allele num: 30244
num of homozygotes: 0

African
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

East Asian
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allele frequency: 2.007226013649137e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -2.433e0

ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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QD
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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allele frequency: 0.0e0
allele num: 3191
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 9.410499428648249e-4
allele num: 29754
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Other
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num of homozygotes: 0

Latino
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allele frequency: 1.986660990492408e-3
allele num: 7047
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African
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allele frequency: 0.0e0
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 6499
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 1.946661475569399e-4
allele num: 5137
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3013
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.586e0

MQRankSum
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DP
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SIO_000300: 8.82587e5

ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.23e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4388
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Latino
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Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.397819401733296e-4
allele num: 7154
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26415
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2951
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QD
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 23748
num of homozygotes: 0

Latino
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Other
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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Latino
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African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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MQRankSum
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FS
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QD
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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South Asian
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Latino
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European (Finnish)
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East Asian
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 1.1477e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.026e-1

QD
type: SiteQuality
SIO_000300: 3.75e0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3613
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17683
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4089
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 297
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2976
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.026e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 4.059e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.1477e1

QD
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 6.33032e5

GenotypeQuality
all individuals: 473
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15533
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4089
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 297
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3613
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.655149013176498e-5
allele num: 17683
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2976
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.026e-1

FS
type: SiteQuality
SIO_000300: 1.1477e1

MQ
type: SiteQuality
SIO_000300: 4.059e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -5.44e-1

DP
type: SiteQuality
SIO_000300: 6.33032e5

QD
type: SiteQuality
SIO_000300: 3.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 27101
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.75e1
variant carriers: 9

African
type: Population
allele count: 1
allele frequency: 2.857142857142857e-4
allele num: 3500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 6.983240223463687e-4
allele num: 2864
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 9.976720984369804e-4
allele num: 6014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 289
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

DP
type: SiteQuality
SIO_000300: 6.25231e5

MQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.05e-1

QD
type: SiteQuality
SIO_000300: 2.031e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

FS
type: SiteQuality
SIO_000300: 1.111e0

MQ
type: SiteQuality
SIO_000300: 4.719e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 289
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2232
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.719e1

QD
type: SiteQuality
SIO_000300: 2.031e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

DP
type: SiteQuality
SIO_000300: 6.25231e5

FS
type: SiteQuality
SIO_000300: 1.111e0

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

MQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.05e-1

GenotypeQuality
all individuals: 6785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1210
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3437
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 281
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2179
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2759
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 4.265e1

VQSLOD
type: SiteQuality
SIO_000300: 8.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.663e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.42e-2

QD
type: SiteQuality
SIO_000300: 9.65e0

DP
type: SiteQuality
SIO_000300: 6.10372e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.558e0

GenotypeQuality
all individuals: 18129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25997
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 467
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3641
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3339
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 279
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2663
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5875
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQ
type: SiteQuality
SIO_000300: 4.498e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.653e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 5.95881e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 2.436e1

GenotypeQuality
all individuals: 1364
bin: 1.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1059
bin: 2.75e1
variant carriers: 11

GenotypeQuality
all individuals: 66
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 149
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 540
bin: 9.75e1
variant carriers: 139

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 149
allele frequency: 1.079788390463077e-2
allele num: 13799
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.059883412824589e-3
allele num: 1887
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 4.327563249001331e-3
allele num: 3004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2263
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.483106931382794e-4
allele num: 2871
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 9.105809506465125e-4
allele num: 5491
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 237
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.911e-1

QD
type: SiteQuality
SIO_000300: 1.713e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 5.42446e5

MQ
type: SiteQuality
SIO_000300: 4.534e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

GenotypeQuality
all individuals: 256
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5247
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 215
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2557
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

DP
type: SiteQuality
SIO_000300: 5.06463e5

MQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.92e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 3.7e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.398e0

QD
type: SiteQuality
SIO_000300: 1.017e1

GenotypeQuality
all individuals: 405
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.905850962454736e-4
allele num: 5247
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1743
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 215
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-2

QD
type: SiteQuality
SIO_000300: 3.037e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.142e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

DP
type: SiteQuality
SIO_000300: 5.05597e5

GenotypeQuality
all individuals: 723
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variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4353
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1083
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 8.130081300813008e-4
allele num: 1230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7220
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.43e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 4.474e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

VQSLOD
type: SiteQuality
SIO_000300: -1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.137e1

DP
type: SiteQuality
SIO_000300: 3.9407e5

GenotypeQuality
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1201
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 963
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 3.8714e5

MQ
type: SiteQuality
SIO_000300: 5.616e1

QD
type: SiteQuality
SIO_000300: 1.234e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 697
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5609
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3875
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.442e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.34414e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.13e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.598e1

GenotypeQuality
all individuals: 1613
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.685284640171858e-4
allele num: 3724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1133
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.32e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

MQ
type: SiteQuality
SIO_000300: 4.898e1

DP
type: SiteQuality
SIO_000300: 3.20069e5

QD
type: SiteQuality
SIO_000300: 2.74e1

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1075
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3581
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4934
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.55e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.7e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 3.05687e5

QD
type: SiteQuality
SIO_000300: 7.93e0

VQSLOD
type: SiteQuality
SIO_000300: -2.591e0

GenotypeQuality
all individuals: 595
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3315
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 349
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4367
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.032520325203252e-3
allele num: 492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 125
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.75122e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.820000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.058e1

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.179e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.82e-1

MQ
type: SiteQuality
SIO_000300: 4.589e1

GenotypeQuality
all individuals: 139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2911
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

DP
type: SiteQuality
SIO_000300: 2.40316e5

MQ
type: SiteQuality
SIO_000300: 4.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.14e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.688e-1

GenotypeQuality
all individuals: 310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25344
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 233
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 8.639308855291577e-4
allele num: 2315
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 773
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 367
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.977e1

MQ
type: SiteQuality
SIO_000300: 5.443e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.29e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.05881e5

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.204e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 511
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3261
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2127
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 399
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.495e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 4.955e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.94238e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.37e-2

QD
type: SiteQuality
SIO_000300: 1.519e1

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 207
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1407
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 373
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.73e-2

DP
type: SiteQuality
SIO_000300: 1.58538e5

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

MQ
type: SiteQuality
SIO_000300: 3.7e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.668e1

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18723
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3136
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 207
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.203e1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.649999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.159999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.58459e5

GenotypeQuality
all individuals: 328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5537
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9899
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24205
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3177
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4617
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20803
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1236
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 8.391608391608392e-4
allele num: 3575
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3081
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 3.954e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.276e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

DP
type: SiteQuality
SIO_000300: 6.17723e5

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25428
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1919
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21299
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4675
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 241
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3167
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3679
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3321
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.88e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.38325e5

VQSLOD
type: SiteQuality
SIO_000300: -1.969e-1

QD
type: SiteQuality
SIO_000300: 2.438e1

GenotypeQuality
all individuals: 26609
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1669
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7537
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8113
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.054653790836244e-4
allele num: 4867
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22487
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1365
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.779e1

VQSLOD
type: SiteQuality
SIO_000300: -2.546e0

DP
type: SiteQuality
SIO_000300: 6.84556e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.595e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.115e0

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 4.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 689
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6675
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 3.25e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 26776
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1110
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 6.061830672863204e-4
allele num: 4949
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1427
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3481
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 2.602585234666435e-4
allele num: 23054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3676
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.317e-1

FS
type: SiteQuality
SIO_000300: 1.846e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.88e-2

DP
type: SiteQuality
SIO_000300: 7.20609e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1665
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1444
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3449
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6427
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.75e1
variant carriers: 32

African
type: Population
allele count: 32
allele frequency: 6.394884092725819e-3
allele num: 5004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3737
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 7.223693715386468e-4
allele num: 4153
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 3.104e0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 7.28071e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.646e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.392e0

GenotypeQuality
all individuals: 1995
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6138
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23961
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3938
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.938360147315371e-4
allele num: 5159
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4307
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 291
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

DP
type: SiteQuality
SIO_000300: 7.34137e5

QD
type: SiteQuality
SIO_000300: 8.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.562e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.738e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 6.952e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 457
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 10545
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 26635
bin: 2.25e1
variant carriers: 25

GenotypeQuality
all individuals: 1386
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3514
bin: 2.75e1
variant carriers: 18

GenotypeQuality
all individuals: 973
bin: 9.75e1
variant carriers: 289

GenotypeQuality
all individuals: 616
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 595
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1175
bin: 1.25e1
variant carriers: 20

GenotypeQuality
all individuals: 1520
bin: 1.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1637
bin: 3.75e1
variant carriers: 25

GenotypeQuality
all individuals: 3443
bin: 3.25e1
variant carriers: 29

GenotypeQuality
all individuals: 5648
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 322
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 424
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 500
bin: 5.25e1
variant carriers: 2

Latino
type: Population
allele count: 3
allele frequency: 6.557377049180328e-4
allele num: 4575
num of homozygotes: 0

East Asian
type: Population
allele count: 292
allele frequency: 7.510288065843622e-2
allele num: 3888
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 75
allele frequency: 2.990430622009569e-3
allele num: 25080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 1.208021261174197e-3
allele num: 4139
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 6.578947368421052e-3
allele num: 304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 28
allele frequency: 1.812297734627832e-2
allele num: 1545
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.092e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 1.463e1

FS
type: SiteQuality
SIO_000300: 7.07e-1

DP
type: SiteQuality
SIO_000300: 7.50701e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.823e0

GenotypeQuality
all individuals: 512
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.75e1
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GenotypeQuality
all individuals: 1082
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 612
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4735
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.16144018583043e-4
allele num: 25830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 317
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.849112426035503e-4
allele num: 5408
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.337540906965872e-4
allele num: 4278
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

QD
type: SiteQuality
SIO_000300: 1.607e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

DP
type: SiteQuality
SIO_000300: 7.68723e5

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 9.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.658e0

GenotypeQuality
all individuals: 12814
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
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variant carriers: 0

GenotypeQuality
all individuals: 4261
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GenotypeQuality
all individuals: 351
bin: 8.25e1
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GenotypeQuality
all individuals: 707
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variant carriers: 1

GenotypeQuality
all individuals: 1723
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
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variant carriers: 0

GenotypeQuality
all individuals: 226
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GenotypeQuality
all individuals: 185
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GenotypeQuality
all individuals: 573
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GenotypeQuality
all individuals: 175
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GenotypeQuality
all individuals: 3409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25710
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5151
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1809
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4277
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.665420423722601e-5
allele num: 27282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5711
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 327
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4617
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 3.069e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.498e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 8.1007e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.609e0

GenotypeQuality
all individuals: 1687
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25077
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3856
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3365
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13382
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.554797198819808e-5
allele num: 28131
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5845
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5391
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4367
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 335
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.044e0

QD
type: SiteQuality
SIO_000300: 1.464e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 3.7e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.399e0

DP
type: SiteQuality
SIO_000300: 8.29544e5

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

GenotypeQuality
all individuals: 2160
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3105
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1092
bin: 9.75e1
variant carriers: 428

GenotypeQuality
all individuals: 695
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3249
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 557
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 24523
bin: 2.25e1
variant carriers: 14

GenotypeQuality
all individuals: 269
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1013
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 598
bin: 4.25e1
variant carriers: 9

GenotypeQuality
all individuals: 3076
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 361
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 615
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 9

GenotypeQuality
all individuals: 15633
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1939
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.008032128514056e-4
allele num: 4980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

African
type: Population
allele count: 488
allele frequency: 7.851971037811746e-2
allele num: 6215
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 3.74187842296833e-4
allele num: 29397
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 2.948829141370338e-3
allele num: 5765
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4543
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.241e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.71577e5

QD
type: SiteQuality
SIO_000300: 1.661e1

GenotypeQuality
all individuals: 605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3008
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2959
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24196
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16579
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2998
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.876720294630742e-4
allele num: 5159
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 359
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30069
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2013
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.139e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 8.85273e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.615e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 723
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19586
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 597
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35317
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 423
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7139
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.42836737608913e-4
allele num: 7001
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6479
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.025435e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.948e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.389e0

QD
type: SiteQuality
SIO_000300: 6.02e0

GenotypeDepth
all individuals: 7162
bin: 2.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 22
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 751
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26175
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2541
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.69483669289641e-5
allele num: 37108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 443
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7231
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5469
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7523
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.405e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

DP
type: SiteQuality
SIO_000300: 1.074598e6

MQ
type: SiteQuality
SIO_000300: 5.888e1

FS
type: SiteQuality
SIO_000300: 1.569e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.039e0

QD
type: SiteQuality
SIO_000300: 1.074e1

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 808
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16088
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.75e1
variant carriers: 0