3-139065779-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065779
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065779
    reference: chr 3
allele count: 6
allele frequency: 4.943072284193702e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.229A>G
  hgvsp: ENSP00000418233.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.218A>G
  hgvsp: ENSP00000419737.1:p.Ile74Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.229A>G
  hgvsp: ENSP00000420482.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.232A>G
  hgvsp: ENSP00000418008.1:p.Ile78Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.232A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.143A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.232A>G
  hgvsp: ENSP00000310785.4:p.Ile78Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000417104
  ensembl transcript: ENST00000495225
  gene symbol: MRPS22
  hgvsc: ENST00000495225.1:c.142A>G
  hgvsp: ENSP00000417104.1:p.Ile48Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.247A>G
  hgvsp: ENSP00000419920.1:p.Ile83Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.109A>G
  hgvsp: ENSP00000419303.1:p.Ile37Val
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile78Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

3-139065782-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065782
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065782
    reference: chr 3
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.235C>G
  hgvsp: ENSP00000418008.1:p.Leu79Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.235C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.250C>G
  hgvsp: ENSP00000419920.1:p.Leu84Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000417104
  ensembl transcript: ENST00000495225
  gene symbol: MRPS22
  hgvsc: ENST00000495225.1:c.145C>G
  hgvsp: ENSP00000417104.1:p.Leu49Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.232C>G
  hgvsp: ENSP00000418233.1:p.Leu78Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.235C>G
  hgvsp: ENSP00000310785.4:p.Leu79Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.112C>G
  hgvsp: ENSP00000419303.1:p.Leu38Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.232C>G
  hgvsp: ENSP00000420482.1:p.Leu78Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.221C>G
  hgvsp: ENSP00000419737.1:p.Leu75Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.146C>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu79Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

3-139065783-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065783
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065783
    reference: chr 3
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.236T>G
  hgvsp: ENSP00000418008.1:p.Leu79Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000417104
  ensembl transcript: ENST00000495225
  gene symbol: MRPS22
  hgvsc: ENST00000495225.1:c.146T>G
  hgvsp: ENSP00000417104.1:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.233T>G
  hgvsp: ENSP00000418233.1:p.Leu78Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.222T>G
  hgvsp: ENSP00000419737.1:p.Leu75Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.113T>G
  hgvsp: ENSP00000419303.1:p.Leu38Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.236T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.233T>G
  hgvsp: ENSP00000420482.1:p.Leu78Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.251T>G
  hgvsp: ENSP00000419920.1:p.Leu84Arg
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.147T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.236T>G
  hgvsp: ENSP00000310785.4:p.Leu79Arg
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu79Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

3-139065784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065784
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065784
    reference: chr 3
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.234C>T
  hgvsp: ENST00000465056.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.114C>T
  hgvsp: ENST00000478464.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.237C>T
  hgvsp: ENST00000310776.4:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.223C>T
  hgvsp: ENST00000466690.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.252C>T
  hgvsp: ENST00000465373.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.237C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000417104
  ensembl transcript: ENST00000495225
  gene symbol: MRPS22
  hgvsc: ENST00000495225.1:c.147C>T
  hgvsp: ENST00000495225.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.234C>T
  hgvsp: ENST00000498505.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.148C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.237C>T
  hgvsp: ENST00000495075.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu79Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-139065786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065786
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.225C>T
  hgvsp: ENSP00000419737.1:p.Thr76Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.239C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000417104
  ensembl transcript: ENST00000495225
  gene symbol: MRPS22
  hgvsc: ENST00000495225.1:c.149C>T
  hgvsp: ENSP00000417104.1:p.Thr50Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.116C>T
  hgvsp: ENSP00000419303.1:p.Thr39Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.236C>T
  hgvsp: ENSP00000420482.1:p.Thr79Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.254C>T
  hgvsp: ENSP00000419920.1:p.Thr85Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.239C>T
  hgvsp: ENSP00000310785.4:p.Thr80Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.239C>T
  hgvsp: ENSP00000418008.1:p.Thr80Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.150C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.236C>T
  hgvsp: ENSP00000418233.1:p.Thr79Met
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr80Met
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-139065798-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065798
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065798
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.237G>C
  hgvsp: ENSP00000419737.1:p.Gly80Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.162G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.266G>C
  hgvsp: ENSP00000419920.1:p.Gly89Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.248G>C
  hgvsp: ENSP00000420482.1:p.Gly83Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.251G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.251G>C
  hgvsp: ENSP00000418008.1:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.128G>C
  hgvsp: ENSP00000419303.1:p.Gly43Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.248G>C
  hgvsp: ENSP00000418233.1:p.Gly83Ala
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.251G>C
  hgvsp: ENSP00000310785.4:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly84Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

3-139065802-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065802
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065802
    reference: chr 3
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.252G>T
  hgvsp: ENSP00000418233.1:p.Leu84Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.166G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.255G>T
  hgvsp: ENSP00000418008.1:p.Leu85Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.255G>T
  hgvsp: ENSP00000310785.4:p.Leu85Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.132G>T
  hgvsp: ENSP00000419303.1:p.Leu44Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.255G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.270G>T
  hgvsp: ENSP00000419920.1:p.Leu90Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.252G>T
  hgvsp: ENSP00000420482.1:p.Leu84Phe
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.241G>T
  hgvsp: ENSP00000419737.1:p.Leu81Phe
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu85Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-139065814-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065814
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065814
    reference: chr 3
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.253G>T
  hgvsp: ENSP00000419737.1:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.282G>T
  hgvsp: ENSP00000419920.1:p.Lys94Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.144G>T
  hgvsp: ENSP00000419303.1:p.Lys48Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.264G>T
  hgvsp: ENSP00000420482.1:p.Lys88Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.7G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.178G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.267G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.267G>T
  hgvsp: ENSP00000418008.1:p.Lys89Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.267G>T
  hgvsp: ENSP00000310785.4:p.Lys89Asn
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.264G>T
  hgvsp: ENSP00000418233.1:p.Lys88Asn
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys89Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

3-139065819-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065819
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065819
    reference: chr 3
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.272T>C
  hgvsp: ENSP00000310785.4:p.Phe91Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.258T>C
  hgvsp: ENSP00000419737.1:p.Phe87Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.272T>C
  hgvsp: ENSP00000418008.1:p.Phe91Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.149T>C
  hgvsp: ENSP00000419303.1:p.Phe50Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.269T>C
  hgvsp: ENSP00000418233.1:p.Phe90Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.287T>C
  hgvsp: ENSP00000419920.1:p.Phe96Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.183T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.12T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.269T>C
  hgvsp: ENSP00000420482.1:p.Phe90Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.272T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe91Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

3-139065828-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065828
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065828
    reference: chr 3
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.281C>G
  hgvsp: ENSP00000310785.4:p.Ala94Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.296C>G
  hgvsp: ENSP00000419920.1:p.Ala99Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.192C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.281C>G
  hgvsp: ENSP00000418008.1:p.Ala94Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.21C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.278C>G
  hgvsp: ENSP00000420482.1:p.Ala93Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.158C>G
  hgvsp: ENSP00000419303.1:p.Ala53Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.281C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.267C>G
  hgvsp: ENSP00000419737.1:p.Ala90Gly
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.278C>G
  hgvsp: ENSP00000418233.1:p.Ala93Gly
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala94Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-139065830-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065830
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065830
    reference: chr 3
allele count: 771
allele frequency: 6.350696846891371e-3
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.160A>C
  hgvsp: ENSP00000419303.1:p.Ile54Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.283A>C
  hgvsp: ENSP00000310785.4:p.Ile95Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.280A>C
  hgvsp: ENSP00000420482.1:p.Ile94Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.283A>C
  hgvsp: ENSP00000418008.1:p.Ile95Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.283A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.298A>C
  hgvsp: ENSP00000419920.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.23A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.280A>C
  hgvsp: ENSP00000418233.1:p.Ile94Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.269A>C
  hgvsp: ENSP00000419737.1:p.Ile91Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.194A>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27894
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 9.75e1
  variant carriers: 489
genotype quality: GenotypeQuality
hgvs: p.Ile95Leu
num of homozygotes: 24
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-139065830-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065830
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065830
    reference: chr 3
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.283A>G
  hgvsp: ENSP00000310785.4:p.Ile95Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.283A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.298A>G
  hgvsp: ENSP00000419920.1:p.Ile100Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.194A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.280A>G
  hgvsp: ENSP00000418233.1:p.Ile94Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.280A>G
  hgvsp: ENSP00000420482.1:p.Ile94Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.283A>G
  hgvsp: ENSP00000418008.1:p.Ile95Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.160A>G
  hgvsp: ENSP00000419303.1:p.Ile54Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.23A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.269A>G
  hgvsp: ENSP00000419737.1:p.Ile91Val
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile95Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

3-139065849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065849
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065849
    reference: chr 3
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.302C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.302C>T
  hgvsp: ENSP00000310785.4:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.302C>T
  hgvsp: ENSP00000418008.1:p.Pro101Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.179C>T
  hgvsp: ENSP00000419303.1:p.Pro60Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.317C>T
  hgvsp: ENSP00000419920.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.299C>T
  hgvsp: ENSP00000418233.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.299C>T
  hgvsp: ENSP00000420482.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.42C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.213C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.288C>T
  hgvsp: ENSP00000419737.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro101Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

3-139065855-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065855
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065855
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.308A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.323A>G
  hgvsp: ENSP00000419920.1:p.Tyr108Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.305A>G
  hgvsp: ENSP00000418233.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.48A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.294A>G
  hgvsp: ENSP00000419737.1:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.308A>G
  hgvsp: ENSP00000418008.1:p.Tyr103Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.308A>G
  hgvsp: ENSP00000310785.4:p.Tyr103Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.305A>G
  hgvsp: ENSP00000420482.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.219A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.185A>G
  hgvsp: ENSP00000419303.1:p.Tyr62Cys
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr103Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

3-139065868-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065868
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065868
    reference: chr 3
allele count: 32
allele frequency: 2.63604461505511e-4
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.61T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.318T>C
  hgvsp: ENST00000465056.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.336T>C
  hgvsp: ENST00000465373.1:c.336T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.232T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.321T>C
  hgvsp: ENST00000495075.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.321T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.307T>C
  hgvsp: ENST00000466690.1:c.307T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.318T>C
  hgvsp: ENST00000498505.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.198T>C
  hgvsp: ENST00000478464.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.321T>C
  hgvsp: ENST00000310776.4:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr107Thr
num of homozygotes: 2
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-139065872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065872
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065872
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.325G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.311G>A
  hgvsp: ENSP00000419737.1:p.Ala105Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.340G>A
  hgvsp: ENSP00000419920.1:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.202G>A
  hgvsp: ENSP00000419303.1:p.Ala68Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.325G>A
  hgvsp: ENSP00000418008.1:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.325G>A
  hgvsp: ENSP00000310785.4:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.236G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.322G>A
  hgvsp: ENSP00000418233.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.322G>A
  hgvsp: ENSP00000420482.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.65G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala109Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

3-139065874-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065874
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065874
    reference: chr 3
allele count: 35
allele frequency: 2.883078798662251e-4
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.313A>G
  hgvsp: ENST00000466690.1:c.313A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.238A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.327A>G
  hgvsp: ENST00000495075.1:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.327A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.324A>G
  hgvsp: ENST00000465056.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.204A>G
  hgvsp: ENST00000478464.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.324A>G
  hgvsp: ENST00000498505.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.67A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.342A>G
  hgvsp: ENST00000465373.1:c.342A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.327A>G
  hgvsp: ENST00000310776.4:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala109Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

3-139065890-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065890
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065890
    reference: chr 3
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+4C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+4C>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.339+4C>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

3-139065890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065890
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065890
    reference: chr 3
allele count: 10
allele frequency: 8.239404126293587e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+4C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+4C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
hgvs: c.339+4C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

3-139065906-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065906
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065906
    reference: chr 3
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+20T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+20T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

3-139065917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065917
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065917
    reference: chr 3
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+31C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+31C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-139065918-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065918
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065918
    reference: chr 3
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+32C>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+32C>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7179
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

3-139065923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065923
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065923
    reference: chr 3
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+37T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+37T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

3-139065929-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065929
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065929
    reference: chr 3
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+43G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+43G>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

3-139065929-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139065929
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139065929
    reference: chr 3
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.339+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.339+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.216+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.339+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.354+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.336+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.250+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.79+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.336+43G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.325+43G>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26675
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10672
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

3-139066953-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066953
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066953
    reference: chr 3
allele count: 6
allele frequency: 5.419173034194982e-5
allele num: 110718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-49A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-49A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12841
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14077
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-139066954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066954
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066954
    reference: chr 3
allele count: 3
allele frequency: 2.705774121976297e-5
allele num: 110874
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-48T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-48T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13388
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5621
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4187
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

3-139066955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066955
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066955
    reference: chr 3
allele count: 1
allele frequency: 9.022013713460844e-6
allele num: 110840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-47A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-47A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12835
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8560
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

3-139066960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066960
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066960
    reference: chr 3
allele count: 8
allele frequency: 7.217090069284065e-5
allele num: 110848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-42G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-42G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12517
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/3-139066962-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066962
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066962
    reference: chr 3
allele count: 6
allele frequency: 5.400637275198473e-5
allele num: 111098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-40A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-40A>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2490
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-139066970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066970
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066970
    reference: chr 3
allele count: 1
allele frequency: 8.934953538241601e-6
allele num: 111920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-32G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-32G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-139066977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066977
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066977
    reference: chr 3
allele count: 1
allele frequency: 8.820208862545865e-6
allele num: 113376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-25C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-25C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5088
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-139066979-TAATA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066979
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066975
    reference: chr 3
allele count: 1
allele frequency: 8.779477094344261e-6
allele num: 113902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-18_251-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-18_337-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-18_340-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-18_217-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-18_337-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-18_340-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-18_355-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-18_80-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-18_326-15delAATA
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-18_340-15delAATA
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: TAATA
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-139066988-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066988
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066988
    reference: chr 3
allele count: 32
allele frequency: 2.748007694421544e-4
allele num: 116448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-14T>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-14T>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32778
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8666
  bin: 9.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

3-139066989-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139066989
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139066989
    reference: chr 3
allele count: 1
allele frequency: 8.566337719298245e-6
allele num: 116736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326-13T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251-13T>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31452
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

3-139067002-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067002
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067002
    reference: chr 3
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.337G>C
  hgvsp: ENSP00000418233.1:p.Ala113Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.217G>C
  hgvsp: ENSP00000419303.1:p.Ala73Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.355G>C
  hgvsp: ENSP00000419920.1:p.Ala119Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.340G>C
  hgvsp: ENSP00000310785.4:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.337G>C
  hgvsp: ENSP00000420482.1:p.Ala113Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.326G>C
  hgvsp: ENSP00000419737.1:p.Ala110Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.251G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.340G>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.340G>C
  hgvsp: ENSP00000418008.1:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.80G>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala114Pro
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-139067007-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067007
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067007
    reference: chr 3
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.345A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.85A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.256A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.331A>C
  hgvsp: ENST00000466690.1:c.331A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.222A>C
  hgvsp: ENST00000478464.1:c.222A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.345A>C
  hgvsp: ENST00000495075.1:c.345A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.342A>C
  hgvsp: ENST00000465056.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.360A>C
  hgvsp: ENST00000465373.1:c.360A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.345A>C
  hgvsp: ENST00000310776.4:c.345A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.342A>C
  hgvsp: ENST00000498505.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr115Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-139067015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067015
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067015
    reference: chr 3
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.368C>T
  hgvsp: ENSP00000419920.1:p.Ala123Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.93C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.350C>T
  hgvsp: ENSP00000418233.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.353C>T
  hgvsp: ENSP00000418008.1:p.Ala118Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.264C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.350C>T
  hgvsp: ENSP00000420482.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.230C>T
  hgvsp: ENSP00000419303.1:p.Ala77Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.339C>T
  hgvsp: ENSP00000419737.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.353C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.353C>T
  hgvsp: ENSP00000310785.4:p.Ala118Val
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala118Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

3-139067023-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067023
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067023
    reference: chr 3
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.361G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.238G>T
  hgvsp: ENSP00000419303.1:p.Ala80Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.358G>T
  hgvsp: ENSP00000418233.1:p.Ala120Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.361G>T
  hgvsp: ENSP00000418008.1:p.Ala121Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.101G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.361G>T
  hgvsp: ENSP00000310785.4:p.Ala121Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.272G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.376G>T
  hgvsp: ENSP00000419920.1:p.Ala126Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.358G>T
  hgvsp: ENSP00000420482.1:p.Ala120Ser
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.347G>T
  hgvsp: ENSP00000419737.1:p.Ala117Ser
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala121Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-139067025-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067025
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067025
    reference: chr 3
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.274A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.363A>G
  hgvsp: ENST00000310776.4:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.360A>G
  hgvsp: ENST00000465056.1:c.360A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.363A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.240A>G
  hgvsp: ENST00000478464.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.349A>G
  hgvsp: ENST00000466690.1:c.349A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.378A>G
  hgvsp: ENST00000465373.1:c.378A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.360A>G
  hgvsp: ENST00000498505.1:c.360A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.363A>G
  hgvsp: ENST00000495075.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.103A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala121Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

3-139067035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067035
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067035
    reference: chr 3
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.250C>T
  hgvsp: ENSP00000419303.1:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.370C>T
  hgvsp: ENSP00000420482.1:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.373C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.373C>T
  hgvsp: ENSP00000418008.1:p.Arg125Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.113C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.373C>T
  hgvsp: ENSP00000310785.4:p.Arg125Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.359C>T
  hgvsp: ENSP00000419737.1:p.Arg121Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.388C>T
  hgvsp: ENSP00000419920.1:p.Arg130Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.370C>T
  hgvsp: ENSP00000418233.1:p.Arg124Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.284C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg125Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

3-139067036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067036
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067036
    reference: chr 3
allele count: 8
allele frequency: 6.597720487571544e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.371G>A
  hgvsp: ENSP00000418233.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.114G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.389G>A
  hgvsp: ENSP00000419920.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.371G>A
  hgvsp: ENSP00000420482.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.374G>A
  hgvsp: ENSP00000310785.4:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.374G>A
  hgvsp: ENSP00000418008.1:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.285G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.251G>A
  hgvsp: ENSP00000419303.1:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.374G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.360G>A
  hgvsp: ENSP00000419737.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg125Gln
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

3-139067040-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067040
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067040
    reference: chr 3
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.375A>G
  hgvsp: ENST00000465056.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.255A>G
  hgvsp: ENST00000478464.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.375A>G
  hgvsp: ENST00000498505.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.289A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.378A>G
  hgvsp: ENST00000310776.4:c.378A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.378A>G
  hgvsp: ENST00000495075.1:c.378A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.118A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.364A>G
  hgvsp: ENST00000466690.1:c.364A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.378A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.393A>G
  hgvsp: ENST00000465373.1:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8733
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Leu126Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-139067052-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067052
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067052
    reference: chr 3
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.387A>G
  hgvsp: ENST00000465056.1:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.130A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.301A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.390A>G
  hgvsp: ENST00000495075.1:c.390A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.405A>G
  hgvsp: ENST00000465373.1:c.405A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.267A>G
  hgvsp: ENST00000478464.1:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.390A>G
  hgvsp: ENST00000310776.4:c.390A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.387A>G
  hgvsp: ENST00000498505.1:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.390A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.376A>G
  hgvsp: ENST00000466690.1:c.376A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro130Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

3-139067063-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067063
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067063
    reference: chr 3
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.141A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.416A>T
  hgvsp: ENSP00000419920.1:p.Glu139Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.401A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.278A>T
  hgvsp: ENSP00000419303.1:p.Glu93Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.312A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.398A>T
  hgvsp: ENSP00000420482.1:p.Glu133Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.398A>T
  hgvsp: ENSP00000418233.1:p.Glu133Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.401A>T
  hgvsp: ENSP00000310785.4:p.Glu134Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.401A>T
  hgvsp: ENSP00000418008.1:p.Glu134Val
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.387A>T
  hgvsp: ENSP00000419737.1:p.Glu130Val
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu134Val
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

3-139067065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067065
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067065
    reference: chr 3
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.280C>T
  hgvsp: ENSP00000419303.1:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.400C>T
  hgvsp: ENSP00000420482.1:p.Arg134Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.314C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.418C>T
  hgvsp: ENSP00000419920.1:p.Arg140Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.400C>T
  hgvsp: ENSP00000418233.1:p.Arg134Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.403C>T
  hgvsp: ENSP00000418008.1:p.Arg135Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.403C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.389C>T
  hgvsp: ENSP00000419737.1:p.Arg131Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.403C>T
  hgvsp: ENSP00000310785.4:p.Arg135Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.143C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg135Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

3-139067066-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067066
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067066
    reference: chr 3
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.419G>T
  hgvsp: ENSP00000419920.1:p.Arg140Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.144G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.281G>T
  hgvsp: ENSP00000419303.1:p.Arg94Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.315G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.401G>T
  hgvsp: ENSP00000418233.1:p.Arg134Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.401G>T
  hgvsp: ENSP00000420482.1:p.Arg134Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.404G>T
  hgvsp: ENSP00000310785.4:p.Arg135Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.390G>T
  hgvsp: ENSP00000419737.1:p.Arg131Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.404G>T
  hgvsp: ENSP00000418008.1:p.Arg135Leu
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.404G>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg135Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

3-139067073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067073
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067073
    reference: chr 3
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.411A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.151A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.426A>G
  hgvsp: ENST00000465373.1:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.397A>G
  hgvsp: ENST00000466690.1:c.397A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.411A>G
  hgvsp: ENST00000310776.4:c.411A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.411A>G
  hgvsp: ENST00000495075.1:c.411A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.408A>G
  hgvsp: ENST00000465056.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.288A>G
  hgvsp: ENST00000478464.1:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.408A>G
  hgvsp: ENST00000498505.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.322A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro137Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/3-139067125-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067125
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067125
    reference: chr 3
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.203A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.463A>C
  hgvsp: ENSP00000310785.4:p.Lys155Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.374A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.340A>C
  hgvsp: ENSP00000419303.1:p.Lys114Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.463A>C
  hgvsp: ENSP00000418008.1:p.Lys155Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.449A>C
  hgvsp: ENSP00000419737.1:p.Lys151Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.2A>C
  hgvsp: ENSP00000420229.1:p.Lys2Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.463A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.460A>C
  hgvsp: ENSP00000418233.1:p.Lys154Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.460A>C
  hgvsp: ENSP00000420482.1:p.Lys154Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.478A>C
  hgvsp: ENSP00000419920.1:p.Lys160Gln
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Lys155Gln
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

3-139067131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067131
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067131
    reference: chr 3
allele count: 2
allele frequency: 1.65144584083365e-5
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.455G>A
  hgvsp: ENSP00000419737.1:p.Val153Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.469G>A
  hgvsp: ENSP00000310785.4:p.Val157Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.466G>A
  hgvsp: ENSP00000418233.1:p.Val156Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.346G>A
  hgvsp: ENSP00000419303.1:p.Val116Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.8G>A
  hgvsp: ENSP00000420229.1:p.Val4Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.469G>A
  hgvsp: ENSP00000418008.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.380G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.466G>A
  hgvsp: ENSP00000420482.1:p.Val156Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.469G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.484G>A
  hgvsp: ENSP00000419920.1:p.Val162Met
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.209G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val157Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-139067138-CTGATA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067138
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067133
    reference: chr 3
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.355_359delGATAT
  hgvsp: ENSP00000419303.1:p.Asp119IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.478_482delGATAT
  hgvsp: ENSP00000310785.4:p.Asp160IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.478_482delGATAT
  hgvsp: ENSP00000418008.1:p.Asp160IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.17_21delGATAT
  hgvsp: ENSP00000420229.1:p.Asp7IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.493_497delGATAT
  hgvsp: ENSP00000419920.1:p.Asp165IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.464_468delGATAT
  hgvsp: ENSP00000419737.1:p.Asp156IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.475_479delGATAT
  hgvsp: ENSP00000420482.1:p.Asp159IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.475_479delGATAT
  hgvsp: ENSP00000418233.1:p.Asp159IlefsTer3
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.218_222delGATAT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.389_393delGATAT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.478_482delGATAT
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp160IlefsTer3
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: CTGATA
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

3-139067144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067144
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067144
    reference: chr 3
allele count: 2
allele frequency: 1.653247805313538e-5
allele num: 120974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.479T>C
  hgvsp: ENSP00000420482.1:p.Ile160Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.482T>C
  hgvsp: ENSP00000310785.4:p.Ile161Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.359T>C
  hgvsp: ENSP00000419303.1:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.222T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.497T>C
  hgvsp: ENSP00000419920.1:p.Ile166Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.482T>C
  hgvsp: ENSP00000418008.1:p.Ile161Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.482T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.393T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.468T>C
  hgvsp: ENSP00000419737.1:p.Ile157Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.21T>C
  hgvsp: ENSP00000420229.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.479T>C
  hgvsp: ENSP00000418233.1:p.Ile160Thr
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile161Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum

3-139067149-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067149
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067149
    reference: chr 3
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.487T>C
  hgvsp: ENSP00000310785.4:p.Tyr163His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.364T>C
  hgvsp: ENSP00000419303.1:p.Tyr122His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.473T>C
  hgvsp: ENSP00000419737.1:p.Tyr159His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.502T>C
  hgvsp: ENSP00000419920.1:p.Tyr168His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.484T>C
  hgvsp: ENSP00000418233.1:p.Tyr162His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.487T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.227T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.484T>C
  hgvsp: ENSP00000420482.1:p.Tyr162His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.487T>C
  hgvsp: ENSP00000418008.1:p.Tyr163His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.26T>C
  hgvsp: ENSP00000420229.1:p.Tyr10His
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.398T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr163His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

3-139067151-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067151
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067151
    reference: chr 3
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.489T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.504T>G
  hgvsp: ENSP00000419920.1:p.Tyr168Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.486T>G
  hgvsp: ENSP00000418233.1:p.Tyr162Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.486T>G
  hgvsp: ENSP00000420482.1:p.Tyr162Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.28T>G
  hgvsp: ENSP00000420229.1:p.Tyr10Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.489T>G
  hgvsp: ENSP00000310785.4:p.Tyr163Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.366T>G
  hgvsp: ENSP00000419303.1:p.Tyr122Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.489T>G
  hgvsp: ENSP00000418008.1:p.Tyr163Ter
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.400T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.229T>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.475T>G
  hgvsp: ENSP00000419737.1:p.Tyr159Ter
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr163Ter
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

3-139067164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067164
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067164
    reference: chr 3
allele count: 2
allele frequency: 1.65708320214758e-5
allele num: 120694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.413C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.488C>T
  hgvsp: ENSP00000419737.1:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.502C>T
  hgvsp: ENSP00000418008.1:p.Arg168Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.517C>T
  hgvsp: ENSP00000419920.1:p.Arg173Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.242C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.41C>T
  hgvsp: ENSP00000420229.1:p.Arg15Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.499C>T
  hgvsp: ENSP00000420482.1:p.Arg167Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.499C>T
  hgvsp: ENSP00000418233.1:p.Arg167Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.379C>T
  hgvsp: ENSP00000419303.1:p.Arg127Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.502C>T
  hgvsp: ENSP00000310785.4:p.Arg168Trp
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.502C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg168Trp
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

3-139067165-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067165
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067165
    reference: chr 3
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.500G>A
  hgvsp: ENSP00000420482.1:p.Arg167Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.380G>A
  hgvsp: ENSP00000419303.1:p.Arg127Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.414G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.503G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.503G>A
  hgvsp: ENSP00000418008.1:p.Arg168Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.503G>A
  hgvsp: ENSP00000310785.4:p.Arg168Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.42G>A
  hgvsp: ENSP00000420229.1:p.Arg15Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.500G>A
  hgvsp: ENSP00000418233.1:p.Arg167Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.489G>A
  hgvsp: ENSP00000419737.1:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.243G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.518G>A
  hgvsp: ENSP00000419920.1:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg168Gln
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/3-139067173-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
allele count: 2
allele frequency: 1.659833684664797e-5
allele num: 120494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+7A>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.422A>C
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.504+7A>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

3-139067173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
allele count: 5
allele frequency: 4.149584211661991e-5
allele num: 120494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.422A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+7A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+7A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.504+7A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-139067173-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067173
    reference: chr 3
allele count: 1
allele frequency: 8.299168423323983e-6
allele num: 120494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.422A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+7A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+7A>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.504+7A>T
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

3-139067184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067184
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067184
    reference: chr 3
allele count: 3
allele frequency: 2.493724127612176e-5
allele num: 120302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.433C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+18C>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+18C>T
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-139067184-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067184
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067183
    reference: chr 3
allele count: 2
allele frequency: 1.662482751741451e-5
allele num: 120302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.434delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+19delG
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+19delG
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: CG
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

3-139067185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067185
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067185
    reference: chr 3
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.434G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+19G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+19G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

3-139067193-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067193
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067193
    reference: chr 3
allele count: 1
allele frequency: 8.325008325008325e-6
allele num: 120120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.442A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+27A>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+27A>T
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-139067212-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067212
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067212
    reference: chr 3
allele count: 6
allele frequency: 5.01311765787143e-5
allele num: 119686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.461T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+46T>C
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+46T>C
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

3-139067216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067216
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067216
    reference: chr 3
allele count: 1
allele frequency: 8.36344172353807e-6
allele num: 119568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.465G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+50G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+50G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32769
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

3-139067217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139067217
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139067217
    reference: chr 3
allele count: 3
allele frequency: 2.50907448605791e-5
allele num: 119566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.501+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.504+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.381+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.501+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.504+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.490+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000486705
  gene symbol: MRPS22
  hgvsc: ENST00000486705.1:n.466A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.519+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.504+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.244+51A>G
  variant of: http://identifiers.org/hgnc/14508
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-139068130-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139068130
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139068130
    reference: chr 3
allele count: 1
allele frequency: 8.135372600065082e-5
allele num: 12292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.502-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.491-40G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.520-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272656
  ensembl transcript: ENST00000608472
  gene symbol: RP11-219D15.3
  hgvsc: ENST00000608472.1:n.84C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.245-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.505-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.502-40G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.505-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.505-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.44-891G>T
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.382-891G>T
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

3-139068141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139068141
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139068141
    reference: chr 3
allele count: 2
allele frequency: 1.626545217957059e-4
allele num: 12296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.502-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.382-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.502-29G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.505-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.505-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.245-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.491-29G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272656
  ensembl transcript: ENST00000608472
  gene symbol: RP11-219D15.3
  hgvsc: ENST00000608472.1:n.73C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.520-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.505-880G>A
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.44-880G>A
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-139068148-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 139068148
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 139068149
    reference: chr 3
allele count: 935
allele frequency: 1.216181061394381e-1
allele num: 7688
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000480938
  gene symbol: MRPS22
  hgvsc: ENST00000480938.1:n.505-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000272656
  ensembl transcript: ENST00000608472
  gene symbol: RP11-219D15.3
  hgvsc: ENST00000608472.1:n.65dupA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl transcript: ENST00000483545
  gene symbol: MRPS22
  hgvsc: ENST00000483545.1:n.245-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420229
  ensembl transcript: ENST00000480644
  gene symbol: MRPS22
  hgvsc: ENST00000480644.1:c.44-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000420482
  ensembl transcript: ENST00000498505
  gene symbol: MRPS22
  hgvsc: ENST00000498505.1:c.502-11dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418008
  ensembl transcript: ENST00000495075
  gene symbol: MRPS22
  hgvsc: ENST00000495075.1:c.505-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419303
  ensembl transcript: ENST00000478464
  gene symbol: MRPS22
  hgvsc: ENST00000478464.1:c.382-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000418233
  ensembl transcript: ENST00000465056
  gene symbol: MRPS22
  hgvsc: ENST00000465056.1:c.502-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000310785
  ensembl transcript: ENST00000310776
  gene symbol: MRPS22
  hgvsc: ENST00000310776.4:c.505-862dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419737
  ensembl transcript: ENST00000466690
  gene symbol: MRPS22
  hgvsc: ENST00000466690.1:c.491-11dupT
  variant of: http://identifiers.org/hgnc/14508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175110
  ensembl protein: ENSP00000419920
  ensembl transcript: ENST00000465373
  gene symbol: MRPS22
  hgvsc: ENST00000465373.1:c.520-862dupT
  variant of: http://identifiers.org/hgnc/14508
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 10417
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2984
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28603
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7299
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991727610598249e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.322e0

DP
type: SiteQuality
SIO_000300: 1.802604e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

GenotypeQuality
all individuals: 7299
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10416
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994485073732166e-5
allele num: 66728
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.354e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

FS
type: SiteQuality
SIO_000300: 5.37e-1

DP
type: SiteQuality
SIO_000300: 1.80271e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10417
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7298
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

FS
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

DP
type: SiteQuality
SIO_000300: 1.802655e6

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

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

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28599
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10418
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 7298
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.372e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 1.802631e6

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

FS
type: SiteQuality
SIO_000300: 8.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.002e1

GenotypeQuality
all individuals: 10419
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.731e0

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.708e0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.138e0

DP
type: SiteQuality
SIO_000300: 1.802804e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
all individuals: 1
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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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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
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
all individuals: 4414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.802864e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.817e0

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

QD
type: SiteQuality
SIO_000300: 1.651e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.423e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.326e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.802961e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.75e1
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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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.272e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.026e1

VQSLOD
type: SiteQuality
SIO_000300: -1.465e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.698e0

DP
type: SiteQuality
SIO_000300: 1.80299e6

GenotypeQuality
all individuals: 7296
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10421
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2085
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.233e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

MQRankSum
type: SiteQuality
SIO_000300: -1.183e0

DP
type: SiteQuality
SIO_000300: 1.803048e6

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
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GenotypeQuality
all individuals: 1475
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.297e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.723e0

DP
type: SiteQuality
SIO_000300: 1.803249e6

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

GenotypeDepth
all individuals: 234
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variant carriers: 28

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11049
bin: 9.75e1
variant carriers: 747

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

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.596367668654659e-4
allele num: 66734
num of homozygotes: 0

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

African
type: Population
allele count: 700
allele frequency: 6.728181468665898e-2
allele num: 10404
num of homozygotes: 23

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 45
allele frequency: 3.88668163758853e-3
allele num: 11578
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.89e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

DP
type: SiteQuality
SIO_000300: 1.868421e6

QD
type: SiteQuality
SIO_000300: 1.466e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

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
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11049
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7205
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.89e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.07e0

DP
type: SiteQuality
SIO_000300: 1.868421e6

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 10650
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variant carriers: 4

GenotypeQuality
all individuals: 1470
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variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.365e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.204e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 3.223e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

DP
type: SiteQuality
SIO_000300: 1.816842e6

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.446e1

FS
type: SiteQuality
SIO_000300: 1.631e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

DP
type: SiteQuality
SIO_000300: 1.81652e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.69e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 30

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2963
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GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.695941853422168e-3
allele num: 16510
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.819178e6

QD
type: SiteQuality
SIO_000300: 1.345e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

GenotypeQuality
all individuals: 2961
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10657
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variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28410
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.184e0

QD
type: SiteQuality
SIO_000300: 9.84e0

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 1.816999e6

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

GenotypeQuality
all individuals: 15
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variant carriers: 0

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

GenotypeQuality
all individuals: 7267
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 35

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 33
allele frequency: 3.171856978085352e-3
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

QD
type: SiteQuality
SIO_000300: 1.319e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

DP
type: SiteQuality
SIO_000300: 1.820259e6

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3379
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10672
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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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.817456e6

FS
type: SiteQuality
SIO_000300: 3.182e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 10

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.452562704471102e-4
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

DP
type: SiteQuality
SIO_000300: 1.817456e6

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.182e0

QD
type: SiteQuality
SIO_000300: 1.281e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 7232
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

DP
type: SiteQuality
SIO_000300: 1.814128e6

QD
type: SiteQuality
SIO_000300: 1.398e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.22e-1

GenotypeQuality
all individuals: 7179
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 189
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 27665
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

Other
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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

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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num of homozygotes: 0

European (Finnish)
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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

DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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FS
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ClippingRankSum
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SIO_000300: 1.03e-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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African
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allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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: 0.0e0
allele num: 66690
num of homozygotes: 0

Latino
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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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Other
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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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Latino
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allele frequency: 0.0e0
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African
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ClippingRankSum
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SIO_000300: -1.524e0

QD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 1.802352e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.075e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 1.617e1

GenotypeQuality
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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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African
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allele count: 1
allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

Latino
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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: 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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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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East Asian
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allele num: 7576
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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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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FS
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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African
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European (Finnish)
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Latino
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1981
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variant carriers: 0

GenotypeQuality
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variant carriers: 7

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7554
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.137426149499101e-4
allele num: 15572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

DP
type: SiteQuality
SIO_000300: 1.468335e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 5.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.363e1

GenotypeQuality
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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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.848620910840282e-4
allele num: 15590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.44e1

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
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SIO_000300: 1.482542e6

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

FS
type: SiteQuality
SIO_000300: 2.525e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

GenotypeQuality
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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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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.04384133611691e-4
allele num: 9580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.983e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.916e1

MQRankSum
type: SiteQuality
SIO_000300: -1.836e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -3.551e0

QD
type: SiteQuality
SIO_000300: 1.223e1

DP
type: SiteQuality
SIO_000300: 1.546644e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

GenotypeQuality
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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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.283038234539389e-4
allele num: 7794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

DP
type: SiteQuality
SIO_000300: 1.604149e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.333e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeQuality
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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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610357821507939e-5
allele num: 62098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 1.618414e6

FS
type: SiteQuality
SIO_000300: 4.629e0

MQ
type: SiteQuality
SIO_000300: 5.826e1

MQRankSum
type: SiteQuality
SIO_000300: -1.409e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.138e1

GenotypeQuality
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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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.867326110849427e-4
allele num: 63690
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.885729518393461e-5
allele num: 11254
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63882
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

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

Other
type: Population
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ClippingRankSum
type: SiteQuality
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QD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 0
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
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.029385034837928e-5
allele num: 66020
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 900
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DP
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.25e1
variant carriers: 0

East Asian
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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

South Asian
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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 frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.602e1

GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

African
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allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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QD
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GenotypeQuality
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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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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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FS
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SIO_000300: 8.59e-1

ClippingRankSum
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SIO_000300: -6.29e-1

MQ
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SIO_000300: 5.909e1

GenotypeQuality
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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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

Other
type: Population
allele count: 0
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
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.757903e6

FS
type: SiteQuality
SIO_000300: 6.17e-1

ReadPosRankSum
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MQ
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SIO_000300: 5.878e1

InbreedingCoeff
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SIO_000300: 2.18e-2

BaseQRankSum
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SIO_000300: -5.27e-1

MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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SIO_000300: 1.339e1

GenotypeQuality
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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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variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

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

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

FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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QD
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GenotypeQuality
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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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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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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele count: 8
allele frequency: 4.849072614862408e-4
allele num: 16498
num of homozygotes: 0

East Asian
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allele count: 0
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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QD
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GenotypeQuality
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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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Other
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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allele frequency: 1.925669170036588e-4
allele num: 10386
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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FS
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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Other
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African
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allele frequency: 9.624639076034648e-5
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 8.34e-1

DP
type: SiteQuality
SIO_000300: 1.762995e6

QD
type: SiteQuality
SIO_000300: 1.234e1

VQSLOD
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SIO_000300: 2.37e0

ClippingRankSum
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SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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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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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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bin: 1.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.23e1

FS
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

BaseQRankSum
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SIO_000300: 7.69e-1

MQ
type: SiteQuality
SIO_000300: 5.844e1

GenotypeQuality
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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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.19e-1

QD
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SIO_000300: 1.547e1

DP
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ClippingRankSum
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SIO_000300: 9.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-2

InbreedingCoeff
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SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.664e0

MQRankSum
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SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.763731e6

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

FS
type: SiteQuality
SIO_000300: 2.989e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.134e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.665e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.743e0

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.97e-1

BaseQRankSum
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SIO_000300: -6.12e-1

DP
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SIO_000300: 1.763774e6

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.49e-1

ClippingRankSum
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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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MQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004446580939791e-5
allele num: 66568
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

African
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Other
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allele num: 908
num of homozygotes: 0

South Asian
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InbreedingCoeff
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SIO_000300: -4.0e-4

MQ
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DP
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QD
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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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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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

East 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

South Asian
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.521e1

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

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

African
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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QD
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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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African
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Other
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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DP
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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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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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Other
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East Asian
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QD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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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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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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QD
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508659706716553e-5
allele num: 66284
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 (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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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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bin: 8.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10014
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South Asian
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allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.020782986950218e-5
allele num: 66208
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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QD
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DP
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 66208
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

Other
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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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African
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allele frequency: 1.997203914519672e-4
allele num: 10014
num of homozygotes: 0

East Asian
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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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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8618
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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Other
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 8.685079034219212e-5
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num of homozygotes: 0

European (Finnish)
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allele num: 6612
num of homozygotes: 0

South Asian
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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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African
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East Asian
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QD
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

African
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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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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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allele frequency: 6.981615080288574e-4
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South Asian
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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FS
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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East Asian
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African
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South Asian
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Other
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 1.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.739849e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.546e1

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3040
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 495
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.676e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 2.37709e5

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.635e0

FS
type: SiteQuality
SIO_000300: 1.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

GenotypeQuality
all individuals: 1081
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.626050420168067e-4
allele num: 7616
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: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.38596e5

VQSLOD
type: SiteQuality
SIO_000300: -1.69e-2

QD
type: SiteQuality
SIO_000300: 2.33e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.129e0