1-216850490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850490
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850490
    reference: chr 1
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.331A>G
  hgvsp: ENSP00000419514.1:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.331A>G
  hgvsp: ENSP00000353108.3:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.400A>G
  hgvsp: ENSP00000386171.3:p.Ile134Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.415A>G
  hgvsp: ENSP00000355904.1:p.Ile139Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24277A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.331A>G
  hgvsp: ENSP00000375761.3:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.331A>G
  hgvsp: ENSP00000355225.3:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.331A>G
  hgvsp: ENSP00000355907.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.331A>G
  hgvsp: ENSP00000354584.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.331A>G
  hgvsp: ENSP00000355905.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.331A>G
  hgvsp: ENSP00000418629.1:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.331A>G
  hgvsp: ENSP00000417374.1:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.331A>G
  hgvsp: ENSP00000419594.1:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.331A>G
  hgvsp: ENSP00000419155.1:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.331A>G
  hgvsp: ENSP00000352077.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile139Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-216850495-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850495
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850493
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.324_325delTG
  hgvsp: ENSP00000419155.1:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.324_325delTG
  hgvsp: ENSP00000355905.2:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.393_394delTG
  hgvsp: ENSP00000386171.3:p.Cys131TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.324_325delTG
  hgvsp: ENSP00000354584.2:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.324_325delTG
  hgvsp: ENSP00000355225.3:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.324_325delTG
  hgvsp: ENSP00000419594.1:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.324_325delTG
  hgvsp: ENSP00000418629.1:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.324_325delTG
  hgvsp: ENSP00000353108.3:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.324_325delTG
  hgvsp: ENSP00000355907.2:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.324_325delTG
  hgvsp: ENSP00000417374.1:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24270_*12+24271delTG
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.324_325delTG
  hgvsp: ENSP00000352077.2:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.324_325delTG
  hgvsp: ENSP00000419514.1:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.324_325delTG
  hgvsp: ENSP00000375761.3:p.Cys108TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.408_409delTG
  hgvsp: ENSP00000355904.1:p.Cys136TrpfsTer2
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 19031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys136TrpfsTer2
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CCA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-216850515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850515
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850515
    reference: chr 1
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.306G>A
  hgvsp: ENST00000361395.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.306G>A
  hgvsp: ENST00000463665.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.306G>A
  hgvsp: ENST00000366938.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.306G>A
  hgvsp: ENST00000361525.3:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.375G>A
  hgvsp: ENST00000408911.3:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24252G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.306G>A
  hgvsp: ENST00000366940.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.306G>A
  hgvsp: ENST00000493603.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.390G>A
  hgvsp: ENST00000366937.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.306G>A
  hgvsp: ENST00000487276.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.306G>A
  hgvsp: ENST00000360012.3:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.306G>A
  hgvsp: ENST00000359162.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.306G>A
  hgvsp: ENST00000493748.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.306G>A
  hgvsp: ENST00000475275.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.306G>A
  hgvsp: ENST00000391890.3:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys130Lys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

1-216850516-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850516
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850516
    reference: chr 1
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.305A>G
  hgvsp: ENSP00000353108.3:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.305A>G
  hgvsp: ENSP00000352077.2:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.305A>G
  hgvsp: ENSP00000355905.2:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.389A>G
  hgvsp: ENSP00000355904.1:p.Lys130Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.305A>G
  hgvsp: ENSP00000355907.2:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.305A>G
  hgvsp: ENSP00000417374.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.374A>G
  hgvsp: ENSP00000386171.3:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.305A>G
  hgvsp: ENSP00000355225.3:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.305A>G
  hgvsp: ENSP00000375761.3:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.305A>G
  hgvsp: ENSP00000419594.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.305A>G
  hgvsp: ENSP00000419514.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.305A>G
  hgvsp: ENSP00000354584.2:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24251A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.305A>G
  hgvsp: ENSP00000418629.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.305A>G
  hgvsp: ENSP00000419155.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys130Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-216850518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850518
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850518
    reference: chr 1
allele count: 8
allele frequency: 6.589351607801793e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.303C>T
  hgvsp: ENST00000361525.3:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.303C>T
  hgvsp: ENST00000366940.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.387C>T
  hgvsp: ENST00000366937.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.303C>T
  hgvsp: ENST00000391890.3:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.303C>T
  hgvsp: ENST00000487276.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.303C>T
  hgvsp: ENST00000493603.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.303C>T
  hgvsp: ENST00000359162.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24249C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.303C>T
  hgvsp: ENST00000360012.3:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.303C>T
  hgvsp: ENST00000361395.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.303C>T
  hgvsp: ENST00000493748.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.303C>T
  hgvsp: ENST00000366938.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.372C>T
  hgvsp: ENST00000408911.3:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.303C>T
  hgvsp: ENST00000475275.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.303C>T
  hgvsp: ENST00000463665.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro129Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

1-216850524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850524
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850524
    reference: chr 1
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.297G>A
  hgvsp: ENST00000493748.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.381G>A
  hgvsp: ENST00000366937.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.297G>A
  hgvsp: ENST00000361395.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24243G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.297G>A
  hgvsp: ENST00000475275.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.366G>A
  hgvsp: ENST00000408911.3:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.297G>A
  hgvsp: ENST00000463665.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.297G>A
  hgvsp: ENST00000360012.3:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.297G>A
  hgvsp: ENST00000366938.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.297G>A
  hgvsp: ENST00000359162.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.297G>A
  hgvsp: ENST00000493603.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.297G>A
  hgvsp: ENST00000361525.3:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.297G>A
  hgvsp: ENST00000487276.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.297G>A
  hgvsp: ENST00000366940.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.297G>A
  hgvsp: ENST00000391890.3:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser127Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

1-216850528-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850528
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850528
    reference: chr 1
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.293A>G
  hgvsp: ENSP00000353108.3:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.293A>G
  hgvsp: ENSP00000355225.3:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.293A>G
  hgvsp: ENSP00000419155.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24239A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.293A>G
  hgvsp: ENSP00000419514.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.362A>G
  hgvsp: ENSP00000386171.3:p.Asn121Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.293A>G
  hgvsp: ENSP00000354584.2:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.293A>G
  hgvsp: ENSP00000355905.2:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.293A>G
  hgvsp: ENSP00000355907.2:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.293A>G
  hgvsp: ENSP00000375761.3:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.293A>G
  hgvsp: ENSP00000417374.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.377A>G
  hgvsp: ENSP00000355904.1:p.Asn126Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.293A>G
  hgvsp: ENSP00000352077.2:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.293A>G
  hgvsp: ENSP00000418629.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.293A>G
  hgvsp: ENSP00000419594.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn126Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

1-216850545-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850545
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850545
    reference: chr 1
allele count: 5
allele frequency: 4.11820907323823e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.276G>C
  hgvsp: ENSP00000353108.3:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.345G>C
  hgvsp: ENSP00000386171.3:p.Lys115Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.276G>C
  hgvsp: ENSP00000375761.3:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.276G>C
  hgvsp: ENSP00000352077.2:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.276G>C
  hgvsp: ENSP00000419594.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.276G>C
  hgvsp: ENSP00000354584.2:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.276G>C
  hgvsp: ENSP00000419155.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.276G>C
  hgvsp: ENSP00000417900.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.276G>C
  hgvsp: ENSP00000418629.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.276G>C
  hgvsp: ENSP00000419514.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.276G>C
  hgvsp: ENSP00000355907.2:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.276G>C
  hgvsp: ENSP00000417374.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.276G>C
  hgvsp: ENSP00000355905.2:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24222G>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.360G>C
  hgvsp: ENSP00000355904.1:p.Lys120Asn
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.276G>C
  hgvsp: ENSP00000355225.3:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19028
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys120Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-216850562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850562
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850562
    reference: chr 1
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.259G>A
  hgvsp: ENSP00000354584.2:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.259G>A
  hgvsp: ENSP00000355905.2:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.259G>A
  hgvsp: ENSP00000375761.3:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.259G>A
  hgvsp: ENSP00000355907.2:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.259G>A
  hgvsp: ENSP00000419155.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.259G>A
  hgvsp: ENSP00000419514.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.343G>A
  hgvsp: ENSP00000355904.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.259G>A
  hgvsp: ENSP00000355225.3:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.259G>A
  hgvsp: ENSP00000418629.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.259G>A
  hgvsp: ENSP00000352077.2:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.259G>A
  hgvsp: ENSP00000353108.3:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.259G>A
  hgvsp: ENSP00000419594.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.328G>A
  hgvsp: ENSP00000386171.3:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.259G>A
  hgvsp: ENSP00000417374.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.259G>A
  hgvsp: ENSP00000417900.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24205G>A
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu115Lys
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

1-216850567-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850567
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850567
    reference: chr 1
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.254T>C
  hgvsp: ENSP00000355225.3:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.254T>C
  hgvsp: ENSP00000355905.2:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.254T>C
  hgvsp: ENSP00000353108.3:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.254T>C
  hgvsp: ENSP00000417374.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24200T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.254T>C
  hgvsp: ENSP00000355907.2:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.254T>C
  hgvsp: ENSP00000417900.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.323T>C
  hgvsp: ENSP00000386171.3:p.Ile108Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.254T>C
  hgvsp: ENSP00000419514.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.254T>C
  hgvsp: ENSP00000354584.2:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.254T>C
  hgvsp: ENSP00000419155.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.254T>C
  hgvsp: ENSP00000352077.2:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.338T>C
  hgvsp: ENSP00000355904.1:p.Ile113Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.254T>C
  hgvsp: ENSP00000375761.3:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.254T>C
  hgvsp: ENSP00000418629.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.254T>C
  hgvsp: ENSP00000419594.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile113Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-216850576-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850576
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850576
    reference: chr 1
allele count: 6
allele frequency: 4.941850887885876e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.245C>A
  hgvsp: ENSP00000418629.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.245C>A
  hgvsp: ENSP00000419155.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.245C>A
  hgvsp: ENSP00000355907.2:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.245C>A
  hgvsp: ENSP00000355905.2:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.245C>A
  hgvsp: ENSP00000354584.2:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.245C>A
  hgvsp: ENSP00000417374.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.245C>A
  hgvsp: ENSP00000417900.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.245C>A
  hgvsp: ENSP00000355225.3:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24191C>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.245C>A
  hgvsp: ENSP00000352077.2:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.245C>A
  hgvsp: ENSP00000353108.3:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.245C>A
  hgvsp: ENSP00000419594.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.245C>A
  hgvsp: ENSP00000419514.1:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.329C>A
  hgvsp: ENSP00000355904.1:p.Ser110Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.314C>A
  hgvsp: ENSP00000386171.3:p.Ser105Tyr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.245C>A
  hgvsp: ENSP00000375761.3:p.Ser82Tyr
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser110Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-216850587-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850587
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850587
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24180T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.234T>C
  hgvsp: ENST00000493748.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.234T>C
  hgvsp: ENST00000493603.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.303T>C
  hgvsp: ENST00000408911.3:c.303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.318T>C
  hgvsp: ENST00000366937.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.234T>C
  hgvsp: ENST00000361525.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.234T>C
  hgvsp: ENST00000469486.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.234T>C
  hgvsp: ENST00000361395.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.234T>C
  hgvsp: ENST00000360012.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.234T>C
  hgvsp: ENST00000359162.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.234T>C
  hgvsp: ENST00000391890.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.234T>C
  hgvsp: ENST00000475275.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.234T>C
  hgvsp: ENST00000366938.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.234T>C
  hgvsp: ENST00000463665.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.234T>C
  hgvsp: ENST00000487276.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.234T>C
  hgvsp: ENST00000366940.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr106Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

1-216850590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850590
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850590
    reference: chr 1
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.231G>A
  hgvsp: ENST00000359162.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.231G>A
  hgvsp: ENST00000475275.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.231G>A
  hgvsp: ENST00000360012.3:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24177G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.231G>A
  hgvsp: ENST00000366938.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.231G>A
  hgvsp: ENST00000469486.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.231G>A
  hgvsp: ENST00000361395.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.231G>A
  hgvsp: ENST00000361525.3:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.300G>A
  hgvsp: ENST00000408911.3:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.231G>A
  hgvsp: ENST00000391890.3:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.231G>A
  hgvsp: ENST00000493748.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.231G>A
  hgvsp: ENST00000493603.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.231G>A
  hgvsp: ENST00000366940.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.231G>A
  hgvsp: ENST00000463665.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.231G>A
  hgvsp: ENST00000487276.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.315G>A
  hgvsp: ENST00000366937.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu105Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-216850599-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850599
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850599
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.222C>T
  hgvsp: ENST00000361395.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.222C>T
  hgvsp: ENST00000359162.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.222C>T
  hgvsp: ENST00000493603.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.222C>T
  hgvsp: ENST00000493748.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.222C>T
  hgvsp: ENST00000366940.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.306C>T
  hgvsp: ENST00000366937.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.291C>T
  hgvsp: ENST00000408911.3:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.222C>T
  hgvsp: ENST00000391890.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.222C>T
  hgvsp: ENST00000487276.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.222C>T
  hgvsp: ENST00000361525.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.222C>T
  hgvsp: ENST00000366938.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.222C>T
  hgvsp: ENST00000469486.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.222C>T
  hgvsp: ENST00000360012.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24168C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.222C>T
  hgvsp: ENST00000475275.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.222C>T
  hgvsp: ENST00000463665.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val102Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

1-216850605-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850605
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850605
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24162G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.216G>A
  hgvsp: ENST00000493603.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.216G>A
  hgvsp: ENST00000366940.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.216G>A
  hgvsp: ENST00000463665.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.216G>A
  hgvsp: ENST00000391890.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.285G>A
  hgvsp: ENST00000408911.3:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.216G>A
  hgvsp: ENST00000366938.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.216G>A
  hgvsp: ENST00000475275.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.216G>A
  hgvsp: ENST00000487276.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.216G>A
  hgvsp: ENST00000493748.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.216G>A
  hgvsp: ENST00000469486.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.216G>A
  hgvsp: ENST00000361525.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.216G>A
  hgvsp: ENST00000361395.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.300G>A
  hgvsp: ENST00000366937.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.216G>A
  hgvsp: ENST00000360012.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.216G>A
  hgvsp: ENST00000359162.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly100Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-216850606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850606
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850606
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.215G>A
  hgvsp: ENSP00000418629.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.284G>A
  hgvsp: ENSP00000386171.3:p.Gly95Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.215G>A
  hgvsp: ENSP00000355905.2:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.215G>A
  hgvsp: ENSP00000419155.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.215G>A
  hgvsp: ENSP00000354584.2:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.215G>A
  hgvsp: ENSP00000355907.2:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.215G>A
  hgvsp: ENSP00000352077.2:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24161G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.215G>A
  hgvsp: ENSP00000417900.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.215G>A
  hgvsp: ENSP00000417374.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.215G>A
  hgvsp: ENSP00000355225.3:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.215G>A
  hgvsp: ENSP00000419594.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.215G>A
  hgvsp: ENSP00000353108.3:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.299G>A
  hgvsp: ENSP00000355904.1:p.Gly100Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.215G>A
  hgvsp: ENSP00000375761.3:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.215G>A
  hgvsp: ENSP00000419514.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly100Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

1-216850610-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850610
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850610
    reference: chr 1
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.211A>G
  hgvsp: ENSP00000417374.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.211A>G
  hgvsp: ENSP00000355905.2:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.211A>G
  hgvsp: ENSP00000355907.2:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.280A>G
  hgvsp: ENSP00000386171.3:p.Ser94Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.211A>G
  hgvsp: ENSP00000417900.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.211A>G
  hgvsp: ENSP00000375761.3:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.211A>G
  hgvsp: ENSP00000419594.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.211A>G
  hgvsp: ENSP00000352077.2:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24157A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.211A>G
  hgvsp: ENSP00000418629.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.211A>G
  hgvsp: ENSP00000419155.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.211A>G
  hgvsp: ENSP00000354584.2:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.211A>G
  hgvsp: ENSP00000353108.3:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.211A>G
  hgvsp: ENSP00000419514.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.211A>G
  hgvsp: ENSP00000355225.3:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.295A>G
  hgvsp: ENSP00000355904.1:p.Ser99Gly
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser99Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

1-216850622-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850622
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850622
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.199A>G
  hgvsp: ENSP00000419155.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.199A>G
  hgvsp: ENSP00000419514.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.199A>G
  hgvsp: ENSP00000417374.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.199A>G
  hgvsp: ENSP00000355905.2:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.199A>G
  hgvsp: ENSP00000419594.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.199A>G
  hgvsp: ENSP00000418629.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.199A>G
  hgvsp: ENSP00000354584.2:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.199A>G
  hgvsp: ENSP00000353108.3:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.199A>G
  hgvsp: ENSP00000355907.2:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.199A>G
  hgvsp: ENSP00000352077.2:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.199A>G
  hgvsp: ENSP00000417900.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.268A>G
  hgvsp: ENSP00000386171.3:p.Ile90Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.199A>G
  hgvsp: ENSP00000375761.3:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24145A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.283A>G
  hgvsp: ENSP00000355904.1:p.Ile95Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.199A>G
  hgvsp: ENSP00000355225.3:p.Ile67Val
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile95Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

1-216850641-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850641
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850641
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.180T>C
  hgvsp: ENST00000366938.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.180T>C
  hgvsp: ENST00000487276.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.180T>C
  hgvsp: ENST00000360012.3:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.180T>C
  hgvsp: ENST00000391890.3:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.180T>C
  hgvsp: ENST00000361525.3:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.180T>C
  hgvsp: ENST00000361395.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.180T>C
  hgvsp: ENST00000493748.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.180T>C
  hgvsp: ENST00000366940.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24126T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.180T>C
  hgvsp: ENST00000359162.2:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.264T>C
  hgvsp: ENST00000366937.1:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.180T>C
  hgvsp: ENST00000493603.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.180T>C
  hgvsp: ENST00000469486.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.180T>C
  hgvsp: ENST00000463665.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.249T>C
  hgvsp: ENST00000408911.3:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.180T>C
  hgvsp: ENST00000475275.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro88Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-216850644-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850644
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850644
    reference: chr 1
allele count: 19
allele frequency: 1.565177276921049e-4
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.246A>G
  hgvsp: ENST00000408911.3:c.246A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.177A>G
  hgvsp: ENST00000366938.2:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.177A>G
  hgvsp: ENST00000391890.3:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.261A>G
  hgvsp: ENST00000366937.1:c.261A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.177A>G
  hgvsp: ENST00000361395.2:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.177A>G
  hgvsp: ENST00000487276.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.177A>G
  hgvsp: ENST00000360012.3:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.177A>G
  hgvsp: ENST00000361525.3:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.177A>G
  hgvsp: ENST00000366940.2:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.177A>G
  hgvsp: ENST00000359162.2:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.177A>G
  hgvsp: ENST00000463665.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24123A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.177A>G
  hgvsp: ENST00000475275.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.177A>G
  hgvsp: ENST00000469486.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.177A>G
  hgvsp: ENST00000493748.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.177A>G
  hgvsp: ENST00000493603.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Pro87Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS

1-216850647-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850647
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850647
    reference: chr 1
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.174G>A
  hgvsp: ENST00000475275.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.174G>A
  hgvsp: ENST00000366940.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.174G>A
  hgvsp: ENST00000487276.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.174G>A
  hgvsp: ENST00000359162.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.174G>A
  hgvsp: ENST00000469486.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.258G>A
  hgvsp: ENST00000366937.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.174G>A
  hgvsp: ENST00000366938.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.174G>A
  hgvsp: ENST00000391890.3:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.174G>A
  hgvsp: ENST00000360012.3:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.174G>A
  hgvsp: ENST00000361525.3:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.243G>A
  hgvsp: ENST00000408911.3:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.174G>A
  hgvsp: ENST00000493748.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.174G>A
  hgvsp: ENST00000361395.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24120G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.174G>A
  hgvsp: ENST00000463665.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.174G>A
  hgvsp: ENST00000493603.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser86Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-216850648-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850648
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850648
    reference: chr 1
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.173C>T
  hgvsp: ENSP00000354584.2:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.173C>T
  hgvsp: ENSP00000419594.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.173C>T
  hgvsp: ENSP00000353108.3:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24119C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.173C>T
  hgvsp: ENSP00000419514.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.173C>T
  hgvsp: ENSP00000355905.2:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.173C>T
  hgvsp: ENSP00000417900.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.173C>T
  hgvsp: ENSP00000419155.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.173C>T
  hgvsp: ENSP00000352077.2:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.242C>T
  hgvsp: ENSP00000386171.3:p.Ser81Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.173C>T
  hgvsp: ENSP00000375761.3:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.173C>T
  hgvsp: ENSP00000418629.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.173C>T
  hgvsp: ENSP00000417374.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.173C>T
  hgvsp: ENSP00000355225.3:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.173C>T
  hgvsp: ENSP00000355907.2:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.257C>T
  hgvsp: ENSP00000355904.1:p.Ser86Leu
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser86Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-216850650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850650
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850650
    reference: chr 1
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.171C>T
  hgvsp: ENST00000487276.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.171C>T
  hgvsp: ENST00000469486.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.171C>T
  hgvsp: ENST00000359162.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.171C>T
  hgvsp: ENST00000391890.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.240C>T
  hgvsp: ENST00000408911.3:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.171C>T
  hgvsp: ENST00000463665.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.171C>T
  hgvsp: ENST00000366940.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.171C>T
  hgvsp: ENST00000361395.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.171C>T
  hgvsp: ENST00000361525.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.171C>T
  hgvsp: ENST00000475275.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.171C>T
  hgvsp: ENST00000360012.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.171C>T
  hgvsp: ENST00000366938.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.171C>T
  hgvsp: ENST00000493603.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.255C>T
  hgvsp: ENST00000366937.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24117C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.171C>T
  hgvsp: ENST00000493748.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp85Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

1-216850658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850658
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850658
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.163G>A
  hgvsp: ENSP00000375761.3:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.163G>A
  hgvsp: ENSP00000353108.3:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24109G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.163G>A
  hgvsp: ENSP00000420370.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.163G>A
  hgvsp: ENSP00000419155.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.163G>A
  hgvsp: ENSP00000419514.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.163G>A
  hgvsp: ENSP00000354584.2:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.163G>A
  hgvsp: ENSP00000355905.2:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.232G>A
  hgvsp: ENSP00000386171.3:p.Gly78Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.163G>A
  hgvsp: ENSP00000417374.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.163G>A
  hgvsp: ENSP00000418629.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.163G>A
  hgvsp: ENSP00000352077.2:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.163G>A
  hgvsp: ENSP00000417900.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.163G>A
  hgvsp: ENSP00000355225.3:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.163G>A
  hgvsp: ENSP00000419594.1:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.163G>A
  hgvsp: ENSP00000355907.2:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.247G>A
  hgvsp: ENSP00000355904.1:p.Gly83Arg
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly83Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-216850659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850659
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850659
    reference: chr 1
allele count: 5
allele frequency: 4.119226903494752e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.162C>T
  hgvsp: ENST00000391890.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.162C>T
  hgvsp: ENST00000366940.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.162C>T
  hgvsp: ENST00000493748.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.162C>T
  hgvsp: ENST00000361395.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.162C>T
  hgvsp: ENST00000360012.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.231C>T
  hgvsp: ENST00000408911.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.162C>T
  hgvsp: ENST00000475275.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.162C>T
  hgvsp: ENST00000487276.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24108C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.162C>T
  hgvsp: ENST00000459955.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.162C>T
  hgvsp: ENST00000361525.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.162C>T
  hgvsp: ENST00000366938.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.246C>T
  hgvsp: ENST00000366937.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.162C>T
  hgvsp: ENST00000493603.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.162C>T
  hgvsp: ENST00000469486.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.162C>T
  hgvsp: ENST00000359162.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.162C>T
  hgvsp: ENST00000463665.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn82Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

1-216850662-C-CTGGAAGTGGGGAGAGTATTCCCAGGTCCGACACTAACCTTGAATTGTCCTCTTGAAGAATGCCTTGCAGGCTTCACA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850662
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850739
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: CTGGAAGTGGGGAGAGTATTCCCAGGTCCGACACTAACCTTGAATTGTCCTCTTGAAGAATGCCTTGCAGGCTTCACA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsp: ENSP00000355905.2:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsp: ENSP00000420370.1:p.Gln53HisfsTer?
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsp: ENSP00000417374.1:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsp: ENSP00000419594.1:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsp: ENSP00000417900.1:p.Gln53HisfsTer?
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsp: ENSP00000355225.3:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsp: ENSP00000419155.1:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsp: ENSP00000354584.2:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsp: ENSP00000353108.3:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsp: ENSP00000355907.2:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsp: ENSP00000418629.1:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsp: ENSP00000386171.3:p.Gln76HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsp: ENSP00000419514.1:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsp: ENSP00000355904.1:p.Gln81HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsp: ENSP00000352077.2:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsp: ENSP00000375761.3:p.Gln53HisfsTer80
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18968
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln81HisfsTer80
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

1-216850665-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850665
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850665
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.156T>A
  hgvsp: ENSP00000420370.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.156T>A
  hgvsp: ENSP00000355907.2:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.225T>A
  hgvsp: ENSP00000386171.3:p.His75Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.156T>A
  hgvsp: ENSP00000353108.3:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.156T>A
  hgvsp: ENSP00000375761.3:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.240T>A
  hgvsp: ENSP00000355904.1:p.His80Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.156T>A
  hgvsp: ENSP00000419514.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.156T>A
  hgvsp: ENSP00000419155.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.156T>A
  hgvsp: ENSP00000355905.2:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.156T>A
  hgvsp: ENSP00000417374.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.156T>A
  hgvsp: ENSP00000417900.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.156T>A
  hgvsp: ENSP00000419594.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.156T>A
  hgvsp: ENSP00000354584.2:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.156T>A
  hgvsp: ENSP00000418629.1:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.156T>A
  hgvsp: ENSP00000355225.3:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.156T>A
  hgvsp: ENSP00000352077.2:p.His52Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24102T>A
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His80Gln
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-216850669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850669
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850669
    reference: chr 1
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.152G>A
  hgvsp: ENSP00000355225.3:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.152G>A
  hgvsp: ENSP00000419514.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.152G>A
  hgvsp: ENSP00000352077.2:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.152G>A
  hgvsp: ENSP00000354584.2:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.152G>A
  hgvsp: ENSP00000355907.2:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.152G>A
  hgvsp: ENSP00000417900.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.152G>A
  hgvsp: ENSP00000420370.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.152G>A
  hgvsp: ENSP00000355905.2:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.152G>A
  hgvsp: ENSP00000418629.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24098G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.152G>A
  hgvsp: ENSP00000375761.3:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.152G>A
  hgvsp: ENSP00000419155.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.152G>A
  hgvsp: ENSP00000353108.3:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.221G>A
  hgvsp: ENSP00000386171.3:p.Gly74Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.152G>A
  hgvsp: ENSP00000419594.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.152G>A
  hgvsp: ENSP00000417374.1:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.236G>A
  hgvsp: ENSP00000355904.1:p.Gly79Asp
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly79Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

1-216850686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850686
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850686
    reference: chr 1
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.135C>T
  hgvsp: ENST00000469486.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.135C>T
  hgvsp: ENST00000366938.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.135C>T
  hgvsp: ENST00000493603.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.204C>T
  hgvsp: ENST00000408911.3:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.135C>T
  hgvsp: ENST00000361395.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.219C>T
  hgvsp: ENST00000366937.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.135C>T
  hgvsp: ENST00000481543.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.135C>T
  hgvsp: ENST00000361525.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.135C>T
  hgvsp: ENST00000366940.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.135C>T
  hgvsp: ENST00000459955.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.135C>T
  hgvsp: ENST00000487276.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.135C>T
  hgvsp: ENST00000463665.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.135C>T
  hgvsp: ENST00000359162.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.135C>T
  hgvsp: ENST00000475275.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.135C>T
  hgvsp: ENST00000360012.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.135C>T
  hgvsp: ENST00000391890.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.135C>T
  hgvsp: ENST00000493748.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24081C>T
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr73Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

1-216850692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850692
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850692
    reference: chr 1
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.213G>A
  hgvsp: ENST00000366937.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.129G>A
  hgvsp: ENST00000487276.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.129G>A
  hgvsp: ENST00000469486.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.129G>A
  hgvsp: ENST00000361525.3:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.129G>A
  hgvsp: ENST00000360012.3:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.129G>A
  hgvsp: ENST00000481543.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24075G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.129G>A
  hgvsp: ENST00000459955.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.129G>A
  hgvsp: ENST00000359162.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.129G>A
  hgvsp: ENST00000493603.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.129G>A
  hgvsp: ENST00000475275.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.129G>A
  hgvsp: ENST00000361395.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.129G>A
  hgvsp: ENST00000366938.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.129G>A
  hgvsp: ENST00000366940.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.129G>A
  hgvsp: ENST00000493748.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.198G>A
  hgvsp: ENST00000408911.3:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.129G>A
  hgvsp: ENST00000391890.3:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.129G>A
  hgvsp: ENST00000463665.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly71Gly
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

1-216850700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850700
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850700
    reference: chr 1
allele count: 6
allele frequency: 4.94266508501384e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24067G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.121G>A
  hgvsp: ENSP00000419155.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.121G>A
  hgvsp: ENSP00000417900.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.121G>A
  hgvsp: ENSP00000352077.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.205G>A
  hgvsp: ENSP00000355904.1:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.121G>A
  hgvsp: ENSP00000355225.3:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.121G>A
  hgvsp: ENSP00000354584.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.121G>A
  hgvsp: ENSP00000353108.3:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.121G>A
  hgvsp: ENSP00000417374.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.121G>A
  hgvsp: ENSP00000419594.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.190G>A
  hgvsp: ENSP00000386171.3:p.Ala64Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.121G>A
  hgvsp: ENSP00000418629.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.121G>A
  hgvsp: ENSP00000355905.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.121G>A
  hgvsp: ENSP00000418895.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.121G>A
  hgvsp: ENSP00000420370.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.121G>A
  hgvsp: ENSP00000355907.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.121G>A
  hgvsp: ENSP00000375761.3:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.121G>A
  hgvsp: ENSP00000419514.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala69Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

1-216850701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850701
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850701
    reference: chr 1
allele count: 21
allele frequency: 1.729932779754844e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.120C>T
  hgvsp: ENST00000361395.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.120C>T
  hgvsp: ENST00000361525.3:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.120C>T
  hgvsp: ENST00000481543.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.120C>T
  hgvsp: ENST00000359162.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.120C>T
  hgvsp: ENST00000493748.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.120C>T
  hgvsp: ENST00000469486.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.204C>T
  hgvsp: ENST00000366937.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.120C>T
  hgvsp: ENST00000366940.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.120C>T
  hgvsp: ENST00000487276.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.189C>T
  hgvsp: ENST00000408911.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.120C>T
  hgvsp: ENST00000360012.3:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.120C>T
  hgvsp: ENST00000493603.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.120C>T
  hgvsp: ENST00000366938.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.120C>T
  hgvsp: ENST00000391890.3:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.120C>T
  hgvsp: ENST00000475275.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.120C>T
  hgvsp: ENST00000459955.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24066C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.120C>T
  hgvsp: ENST00000463665.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp68Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-216850710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850710
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.111C>T
  hgvsp: ENST00000366938.2:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.111C>T
  hgvsp: ENST00000481543.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.195C>T
  hgvsp: ENST00000366937.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.111C>T
  hgvsp: ENST00000361395.2:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.111C>T
  hgvsp: ENST00000459955.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.111C>T
  hgvsp: ENST00000487276.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.111C>T
  hgvsp: ENST00000359162.2:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.111C>T
  hgvsp: ENST00000493748.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.111C>T
  hgvsp: ENST00000360012.3:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24057C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.111C>T
  hgvsp: ENST00000469486.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.111C>T
  hgvsp: ENST00000493603.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.180C>T
  hgvsp: ENST00000408911.3:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.111C>T
  hgvsp: ENST00000366940.2:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.111C>T
  hgvsp: ENST00000463665.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.111C>T
  hgvsp: ENST00000475275.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.111C>T
  hgvsp: ENST00000391890.3:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.111C>T
  hgvsp: ENST00000361525.3:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly65Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-216850716-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850716
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850716
    reference: chr 1
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.105T>C
  hgvsp: ENST00000487276.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.105T>C
  hgvsp: ENST00000475275.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.105T>C
  hgvsp: ENST00000360012.3:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.105T>C
  hgvsp: ENST00000463665.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.174T>C
  hgvsp: ENST00000408911.3:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.105T>C
  hgvsp: ENST00000493748.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.105T>C
  hgvsp: ENST00000361395.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.105T>C
  hgvsp: ENST00000366938.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.105T>C
  hgvsp: ENST00000361525.3:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.105T>C
  hgvsp: ENST00000391890.3:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.105T>C
  hgvsp: ENST00000481543.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.105T>C
  hgvsp: ENST00000366940.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.105T>C
  hgvsp: ENST00000359162.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.105T>C
  hgvsp: ENST00000459955.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.105T>C
  hgvsp: ENST00000469486.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24051T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.105T>C
  hgvsp: ENST00000493603.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.189T>C
  hgvsp: ENST00000366937.1:c.189T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro63Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-216850728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850728
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850728
    reference: chr 1
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.93C>T
  hgvsp: ENST00000493748.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.93C>T
  hgvsp: ENST00000459955.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.93C>T
  hgvsp: ENST00000360012.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.93C>T
  hgvsp: ENST00000366940.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.93C>T
  hgvsp: ENST00000361395.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.93C>T
  hgvsp: ENST00000391890.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.162C>T
  hgvsp: ENST00000408911.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.93C>T
  hgvsp: ENST00000493603.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.93C>T
  hgvsp: ENST00000361525.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.177C>T
  hgvsp: ENST00000366937.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.93C>T
  hgvsp: ENST00000359162.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24039C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.93C>T
  hgvsp: ENST00000481543.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.93C>T
  hgvsp: ENST00000487276.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.93C>T
  hgvsp: ENST00000463665.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.93C>T
  hgvsp: ENST00000366938.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.93C>T
  hgvsp: ENST00000475275.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.93C>T
  hgvsp: ENST00000469486.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn59Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

1-216850733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850733
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850733
    reference: chr 1
allele count: 13
allele frequency: 1.071175491504754e-4
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.88G>A
  hgvsp: ENSP00000355907.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24034G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.88G>A
  hgvsp: ENSP00000419514.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.88G>A
  hgvsp: ENSP00000354584.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.88G>A
  hgvsp: ENSP00000419594.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.88G>A
  hgvsp: ENSP00000355905.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.88G>A
  hgvsp: ENSP00000420370.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.88G>A
  hgvsp: ENSP00000417374.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.88G>A
  hgvsp: ENSP00000375761.3:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.172G>A
  hgvsp: ENSP00000355904.1:p.Val58Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.88G>A
  hgvsp: ENSP00000419155.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.88G>A
  hgvsp: ENSP00000417900.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.88G>A
  hgvsp: ENSP00000355225.3:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.88G>A
  hgvsp: ENSP00000352077.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.88G>A
  hgvsp: ENSP00000353108.3:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.88G>A
  hgvsp: ENSP00000418895.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.157G>A
  hgvsp: ENSP00000386171.3:p.Val53Ile
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.88G>A
  hgvsp: ENSP00000418629.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Val58Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-216850740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850740
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850740
    reference: chr 1
allele count: 10
allele frequency: 8.241169586787757e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.81G>A
  hgvsp: ENST00000493603.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.81G>A
  hgvsp: ENST00000360012.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.81G>A
  hgvsp: ENST00000493748.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.81G>A
  hgvsp: ENST00000469486.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.81G>A
  hgvsp: ENST00000366938.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.81G>A
  hgvsp: ENST00000487276.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.165G>A
  hgvsp: ENST00000366937.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.81G>A
  hgvsp: ENST00000361395.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.150G>A
  hgvsp: ENST00000408911.3:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.81G>A
  hgvsp: ENST00000359162.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.81G>A
  hgvsp: ENST00000459955.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.81G>A
  hgvsp: ENST00000481543.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.81G>A
  hgvsp: ENST00000366940.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.81G>A
  hgvsp: ENST00000475275.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.81G>A
  hgvsp: ENST00000391890.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24027G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.81G>A
  hgvsp: ENST00000361525.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.81G>A
  hgvsp: ENST00000463665.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr55Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-216850741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850741
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850741
    reference: chr 1
allele count: 5
allele frequency: 4.120652711389484e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.80C>T
  hgvsp: ENSP00000417900.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.80C>T
  hgvsp: ENSP00000419594.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.164C>T
  hgvsp: ENSP00000355904.1:p.Thr55Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.80C>T
  hgvsp: ENSP00000354584.2:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.80C>T
  hgvsp: ENSP00000353108.3:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.80C>T
  hgvsp: ENSP00000418895.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.80C>T
  hgvsp: ENSP00000352077.2:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.149C>T
  hgvsp: ENSP00000386171.3:p.Thr50Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.80C>T
  hgvsp: ENSP00000355225.3:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.80C>T
  hgvsp: ENSP00000419155.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.80C>T
  hgvsp: ENSP00000355907.2:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.80C>T
  hgvsp: ENSP00000375761.3:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.80C>T
  hgvsp: ENSP00000355905.2:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.80C>T
  hgvsp: ENSP00000420370.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.80C>T
  hgvsp: ENSP00000419514.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24026C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.80C>T
  hgvsp: ENSP00000417374.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.80C>T
  hgvsp: ENSP00000418629.1:p.Thr27Met
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr55Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ

1-216850750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850750
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850750
    reference: chr 1
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.71C>T
  hgvsp: ENSP00000418629.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24017C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.71C>T
  hgvsp: ENSP00000418895.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.71C>T
  hgvsp: ENSP00000419155.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.71C>T
  hgvsp: ENSP00000353108.3:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.71C>T
  hgvsp: ENSP00000419594.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.71C>T
  hgvsp: ENSP00000355225.3:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.71C>T
  hgvsp: ENSP00000352077.2:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.71C>T
  hgvsp: ENSP00000354584.2:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.71C>T
  hgvsp: ENSP00000355907.2:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.71C>T
  hgvsp: ENSP00000417374.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.155C>T
  hgvsp: ENSP00000355904.1:p.Ala52Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.71C>T
  hgvsp: ENSP00000419514.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.140C>T
  hgvsp: ENSP00000386171.3:p.Ala47Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.71C>T
  hgvsp: ENSP00000355905.2:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.71C>T
  hgvsp: ENSP00000420370.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.71C>T
  hgvsp: ENSP00000417900.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.71C>T
  hgvsp: ENSP00000375761.3:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala52Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-216850752-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850752
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850752
    reference: chr 1
allele count: 234
allele frequency: 1.929165017807677e-3
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.69A>G
  hgvsp: ENST00000366940.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.69A>G
  hgvsp: ENST00000361395.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.69A>G
  hgvsp: ENST00000469486.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.69A>G
  hgvsp: ENST00000391890.3:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.69A>G
  hgvsp: ENST00000459955.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.69A>G
  hgvsp: ENST00000366938.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.153A>G
  hgvsp: ENST00000366937.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.69A>G
  hgvsp: ENST00000361525.3:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.69A>G
  hgvsp: ENST00000475275.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.138A>G
  hgvsp: ENST00000408911.3:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.69A>G
  hgvsp: ENST00000493603.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24015A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.69A>G
  hgvsp: ENST00000359162.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.69A>G
  hgvsp: ENST00000360012.3:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.69A>G
  hgvsp: ENST00000463665.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.69A>G
  hgvsp: ENST00000487276.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.69A>G
  hgvsp: ENST00000481543.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.69A>G
  hgvsp: ENST00000493748.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro51Pro
num of homozygotes: 2
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-216850762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850762
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850762
    reference: chr 1
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.59C>T
  hgvsp: ENSP00000418895.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.59C>T
  hgvsp: ENSP00000352077.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.128C>T
  hgvsp: ENSP00000386171.3:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.59C>T
  hgvsp: ENSP00000419155.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.59C>T
  hgvsp: ENSP00000353108.3:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.59C>T
  hgvsp: ENSP00000420370.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.59C>T
  hgvsp: ENSP00000417374.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.59C>T
  hgvsp: ENSP00000355907.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.143C>T
  hgvsp: ENSP00000355904.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.59C>T
  hgvsp: ENSP00000355225.3:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.59C>T
  hgvsp: ENSP00000354584.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.59C>T
  hgvsp: ENSP00000417900.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.59C>T
  hgvsp: ENSP00000419514.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.59C>T
  hgvsp: ENSP00000375761.3:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.59C>T
  hgvsp: ENSP00000418629.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24005C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.59C>T
  hgvsp: ENSP00000419594.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.59C>T
  hgvsp: ENSP00000355905.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro48Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

1-216850763-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850763
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850763
    reference: chr 1
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.58C>G
  hgvsp: ENSP00000375761.3:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.58C>G
  hgvsp: ENSP00000354584.2:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.127C>G
  hgvsp: ENSP00000386171.3:p.Pro43Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.58C>G
  hgvsp: ENSP00000352077.2:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.58C>G
  hgvsp: ENSP00000417900.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.58C>G
  hgvsp: ENSP00000419594.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.58C>G
  hgvsp: ENSP00000418629.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.58C>G
  hgvsp: ENSP00000420370.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.58C>G
  hgvsp: ENSP00000355907.2:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.58C>G
  hgvsp: ENSP00000355225.3:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.58C>G
  hgvsp: ENSP00000355905.2:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.58C>G
  hgvsp: ENSP00000419155.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.58C>G
  hgvsp: ENSP00000418895.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.58C>G
  hgvsp: ENSP00000353108.3:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.58C>G
  hgvsp: ENSP00000419514.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.142C>G
  hgvsp: ENSP00000355904.1:p.Pro48Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.58C>G
  hgvsp: ENSP00000417374.1:p.Pro20Ala
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24004C>G
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro48Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-216850763-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850763
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850763
    reference: chr 1
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.58C>A
  hgvsp: ENSP00000417374.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.142C>A
  hgvsp: ENSP00000355904.1:p.Pro48Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.58C>A
  hgvsp: ENSP00000355905.2:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.127C>A
  hgvsp: ENSP00000386171.3:p.Pro43Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.58C>A
  hgvsp: ENSP00000355225.3:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.58C>A
  hgvsp: ENSP00000354584.2:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.58C>A
  hgvsp: ENSP00000375761.3:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24004C>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.58C>A
  hgvsp: ENSP00000353108.3:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.58C>A
  hgvsp: ENSP00000418895.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.58C>A
  hgvsp: ENSP00000419155.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.58C>A
  hgvsp: ENSP00000420370.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.58C>A
  hgvsp: ENSP00000355907.2:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.58C>A
  hgvsp: ENSP00000418629.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.58C>A
  hgvsp: ENSP00000352077.2:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.58C>A
  hgvsp: ENSP00000419514.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.58C>A
  hgvsp: ENSP00000417900.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.58C>A
  hgvsp: ENSP00000419594.1:p.Pro20Thr
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro48Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

1-216850767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850767
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850767
    reference: chr 1
allele count: 3
allele frequency: 2.477700693756194e-5
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.54G>A
  hgvsp: ENST00000391890.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.54G>A
  hgvsp: ENST00000487276.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.54G>A
  hgvsp: ENST00000463665.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.54G>A
  hgvsp: ENST00000475275.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.54G>A
  hgvsp: ENST00000481543.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.54G>A
  hgvsp: ENST00000493748.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.54G>A
  hgvsp: ENST00000360012.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.54G>A
  hgvsp: ENST00000361525.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.54G>A
  hgvsp: ENST00000469486.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.54G>A
  hgvsp: ENST00000493603.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.54G>A
  hgvsp: ENST00000361395.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+24000G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.54G>A
  hgvsp: ENST00000359162.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.54G>A
  hgvsp: ENST00000459955.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.54G>A
  hgvsp: ENST00000366938.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.138G>A
  hgvsp: ENST00000366937.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.54G>A
  hgvsp: ENST00000366940.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.123G>A
  hgvsp: ENST00000408911.3:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr46Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-216850768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850768
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850768
    reference: chr 1
allele count: 3
allele frequency: 2.478232854759033e-5
allele num: 121054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.53C>T
  hgvsp: ENSP00000420370.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.53C>T
  hgvsp: ENSP00000418895.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.53C>T
  hgvsp: ENSP00000417374.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.122C>T
  hgvsp: ENSP00000386171.3:p.Thr41Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.53C>T
  hgvsp: ENSP00000355905.2:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.53C>T
  hgvsp: ENSP00000419514.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.53C>T
  hgvsp: ENSP00000375761.3:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.53C>T
  hgvsp: ENSP00000353108.3:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.53C>T
  hgvsp: ENSP00000419155.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.53C>T
  hgvsp: ENSP00000354584.2:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.53C>T
  hgvsp: ENSP00000417900.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23999C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.137C>T
  hgvsp: ENSP00000355904.1:p.Thr46Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.53C>T
  hgvsp: ENSP00000352077.2:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.53C>T
  hgvsp: ENSP00000418629.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.53C>T
  hgvsp: ENSP00000355907.2:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.53C>T
  hgvsp: ENSP00000355225.3:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.53C>T
  hgvsp: ENSP00000419594.1:p.Thr18Met
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr46Met
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-216850775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850775
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850775
    reference: chr 1
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.46A>G
  hgvsp: ENSP00000355225.3:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.46A>G
  hgvsp: ENSP00000419594.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.46A>G
  hgvsp: ENSP00000353108.3:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.46A>G
  hgvsp: ENSP00000419514.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.46A>G
  hgvsp: ENSP00000375761.3:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.46A>G
  hgvsp: ENSP00000355907.2:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.46A>G
  hgvsp: ENSP00000419155.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.46A>G
  hgvsp: ENSP00000352077.2:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23992A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.115A>G
  hgvsp: ENSP00000386171.3:p.Ile39Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.46A>G
  hgvsp: ENSP00000418629.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.46A>G
  hgvsp: ENSP00000420370.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.46A>G
  hgvsp: ENSP00000355905.2:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.46A>G
  hgvsp: ENSP00000354584.2:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.46A>G
  hgvsp: ENSP00000417374.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.46A>G
  hgvsp: ENSP00000417900.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.130A>G
  hgvsp: ENSP00000355904.1:p.Ile44Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.46A>G
  hgvsp: ENSP00000418895.1:p.Ile16Val
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile44Val
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-216850780-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850780
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850780
    reference: chr 1
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.41C>T
  hgvsp: ENSP00000417900.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.41C>T
  hgvsp: ENSP00000354584.2:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.41C>T
  hgvsp: ENSP00000419514.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.41C>T
  hgvsp: ENSP00000355225.3:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.41C>T
  hgvsp: ENSP00000375761.3:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.41C>T
  hgvsp: ENSP00000418895.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.41C>T
  hgvsp: ENSP00000353108.3:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.41C>T
  hgvsp: ENSP00000418629.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.41C>T
  hgvsp: ENSP00000419155.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.41C>T
  hgvsp: ENSP00000419594.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.41C>T
  hgvsp: ENSP00000420370.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.41C>T
  hgvsp: ENSP00000355905.2:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.41C>T
  hgvsp: ENSP00000417374.1:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.41C>T
  hgvsp: ENSP00000355907.2:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.110C>T
  hgvsp: ENSP00000386171.3:p.Ser37Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.41C>T
  hgvsp: ENSP00000352077.2:p.Ser14Phe
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23987C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.125C>T
  hgvsp: ENSP00000355904.1:p.Ser42Phe
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser42Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-216850782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850782
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850782
    reference: chr 1
allele count: 8
allele frequency: 6.652806652806653e-5
allele num: 120250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.39G>A
  hgvsp: ENST00000493603.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.39G>A
  hgvsp: ENST00000366938.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.39G>A
  hgvsp: ENST00000475275.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.39G>A
  hgvsp: ENST00000361395.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.39G>A
  hgvsp: ENST00000359162.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.39G>A
  hgvsp: ENST00000391890.3:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.123G>A
  hgvsp: ENST00000366937.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.39G>A
  hgvsp: ENST00000360012.3:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.39G>A
  hgvsp: ENST00000487276.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.39G>A
  hgvsp: ENST00000366940.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.39G>A
  hgvsp: ENST00000361525.3:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.39G>A
  hgvsp: ENST00000463665.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.39G>A
  hgvsp: ENST00000493748.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.39G>A
  hgvsp: ENST00000459955.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.39G>A
  hgvsp: ENST00000469486.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.39G>A
  hgvsp: ENST00000481543.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23985G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.108G>A
  hgvsp: ENST00000408911.3:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser41Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-216850783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850783
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850783
    reference: chr 1
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.38C>T
  hgvsp: ENSP00000375761.3:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.38C>T
  hgvsp: ENSP00000354584.2:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.38C>T
  hgvsp: ENSP00000417900.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.38C>T
  hgvsp: ENSP00000417374.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.38C>T
  hgvsp: ENSP00000419594.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23984C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.38C>T
  hgvsp: ENSP00000419155.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.38C>T
  hgvsp: ENSP00000419514.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.38C>T
  hgvsp: ENSP00000420370.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.38C>T
  hgvsp: ENSP00000355905.2:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.38C>T
  hgvsp: ENSP00000355907.2:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.38C>T
  hgvsp: ENSP00000418629.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.122C>T
  hgvsp: ENSP00000355904.1:p.Ser41Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.38C>T
  hgvsp: ENSP00000353108.3:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.107C>T
  hgvsp: ENSP00000386171.3:p.Ser36Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.38C>T
  hgvsp: ENSP00000418895.1:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.38C>T
  hgvsp: ENSP00000352077.2:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.38C>T
  hgvsp: ENSP00000355225.3:p.Ser13Leu
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser41Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-216850798-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850798
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850798
    reference: chr 1
allele count: 1
allele frequency: 8.454943605526151e-6
allele num: 118274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.23T>C
  hgvsp: ENSP00000419155.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23969T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.107T>C
  hgvsp: ENSP00000355904.1:p.Ile36Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.23T>C
  hgvsp: ENSP00000418895.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.23T>C
  hgvsp: ENSP00000355905.2:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.23T>C
  hgvsp: ENSP00000419514.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.23T>C
  hgvsp: ENSP00000354584.2:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.92T>C
  hgvsp: ENSP00000386171.3:p.Ile31Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.23T>C
  hgvsp: ENSP00000417900.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.23T>C
  hgvsp: ENSP00000355225.3:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.23T>C
  hgvsp: ENSP00000420370.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.23T>C
  hgvsp: ENSP00000355907.2:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.23T>C
  hgvsp: ENSP00000353108.3:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.23T>C
  hgvsp: ENSP00000375761.3:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.23T>C
  hgvsp: ENSP00000418629.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.23T>C
  hgvsp: ENSP00000352077.2:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.23T>C
  hgvsp: ENSP00000419594.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.23T>C
  hgvsp: ENSP00000417374.1:p.Ile8Thr
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile36Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

1-216850799-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850799
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850799
    reference: chr 1
allele count: 1
allele frequency: 8.479031355457952e-6
allele num: 117938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.22A>G
  hgvsp: ENSP00000353108.3:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.22A>G
  hgvsp: ENSP00000420370.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.22A>G
  hgvsp: ENSP00000355907.2:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.22A>G
  hgvsp: ENSP00000355905.2:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.22A>G
  hgvsp: ENSP00000354584.2:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.22A>G
  hgvsp: ENSP00000418895.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23968A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.22A>G
  hgvsp: ENSP00000375761.3:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.22A>G
  hgvsp: ENSP00000355225.3:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.91A>G
  hgvsp: ENSP00000386171.3:p.Ile31Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.22A>G
  hgvsp: ENSP00000419594.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.22A>G
  hgvsp: ENSP00000419514.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.22A>G
  hgvsp: ENSP00000417900.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.22A>G
  hgvsp: ENSP00000417374.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.22A>G
  hgvsp: ENSP00000419155.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.22A>G
  hgvsp: ENSP00000418629.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.106A>G
  hgvsp: ENSP00000355904.1:p.Ile36Val
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.22A>G
  hgvsp: ENSP00000352077.2:p.Ile8Val
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile36Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

1-216850804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850804
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850804
    reference: chr 1
allele count: 2
allele frequency: 1.708905104499547e-5
allele num: 117034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.17G>A
  hgvsp: ENSP00000417900.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.17G>A
  hgvsp: ENSP00000375761.3:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.17G>A
  hgvsp: ENSP00000419514.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.17G>A
  hgvsp: ENSP00000352077.2:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.17G>A
  hgvsp: ENSP00000419155.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.17G>A
  hgvsp: ENSP00000355225.3:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.17G>A
  hgvsp: ENSP00000355905.2:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.101G>A
  hgvsp: ENSP00000355904.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.17G>A
  hgvsp: ENSP00000420370.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.17G>A
  hgvsp: ENSP00000417374.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.17G>A
  hgvsp: ENSP00000418895.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.17G>A
  hgvsp: ENSP00000354584.2:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.17G>A
  hgvsp: ENSP00000418629.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23963G>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.17G>A
  hgvsp: ENSP00000353108.3:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.86G>A
  hgvsp: ENSP00000386171.3:p.Arg29Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.17G>A
  hgvsp: ENSP00000419594.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.17G>A
  hgvsp: ENSP00000355907.2:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg34Gln
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

1-216850810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850810
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850810
    reference: chr 1
allele count: 1
allele frequency: 8.696710903936131e-6
allele num: 114986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.11A>G
  hgvsp: ENSP00000355907.2:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.11A>G
  hgvsp: ENSP00000355225.3:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.11A>G
  hgvsp: ENSP00000418895.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.11A>G
  hgvsp: ENSP00000419155.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.11A>G
  hgvsp: ENSP00000419594.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.11A>G
  hgvsp: ENSP00000417900.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.80A>G
  hgvsp: ENSP00000386171.3:p.Lys27Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.11A>G
  hgvsp: ENSP00000354584.2:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.11A>G
  hgvsp: ENSP00000417374.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.11A>G
  hgvsp: ENSP00000352077.2:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.11A>G
  hgvsp: ENSP00000355905.2:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.11A>G
  hgvsp: ENSP00000353108.3:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.11A>G
  hgvsp: ENSP00000420370.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.11A>G
  hgvsp: ENSP00000418629.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.95A>G
  hgvsp: ENSP00000355904.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23957A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.11A>G
  hgvsp: ENSP00000375761.3:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.11A>G
  hgvsp: ENSP00000419514.1:p.Lys4Arg
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys32Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

1-216850812-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850812
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850812
    reference: chr 1
allele count: 1
allele frequency: 8.700494188069882e-6
allele num: 114936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.9C>A
  hgvsp: ENSP00000419155.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.9C>A
  hgvsp: ENSP00000355907.2:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.9C>A
  hgvsp: ENSP00000417374.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.9C>A
  hgvsp: ENSP00000417900.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.9C>A
  hgvsp: ENSP00000354584.2:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.9C>A
  hgvsp: ENSP00000355225.3:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.9C>A
  hgvsp: ENSP00000420370.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.93C>A
  hgvsp: ENSP00000355904.1:p.Asn31Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.9C>A
  hgvsp: ENSP00000419514.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.9C>A
  hgvsp: ENSP00000353108.3:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.9C>A
  hgvsp: ENSP00000355905.2:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.9C>A
  hgvsp: ENSP00000418895.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.78C>A
  hgvsp: ENSP00000386171.3:p.Asn26Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.9C>A
  hgvsp: ENSP00000419594.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.9C>A
  hgvsp: ENSP00000375761.3:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23955C>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.9C>A
  hgvsp: ENSP00000352077.2:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.9C>A
  hgvsp: ENSP00000418629.1:p.Asn3Lys
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn31Lys
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-216850814-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850814
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850814
    reference: chr 1
allele count: 1
allele frequency: 8.754727552878554e-6
allele num: 114224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23953A>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.7A>G
  hgvsp: ENSP00000355907.2:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.7A>G
  hgvsp: ENSP00000355225.3:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.7A>G
  hgvsp: ENSP00000418895.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.7A>G
  hgvsp: ENSP00000417900.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.7A>G
  hgvsp: ENSP00000354584.2:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.7A>G
  hgvsp: ENSP00000352077.2:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.7A>G
  hgvsp: ENSP00000419155.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.7A>G
  hgvsp: ENSP00000355905.2:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.7A>G
  hgvsp: ENSP00000417374.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.7A>G
  hgvsp: ENSP00000420370.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.76A>G
  hgvsp: ENSP00000386171.3:p.Asn26Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.7A>G
  hgvsp: ENSP00000419514.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.7A>G
  hgvsp: ENSP00000353108.3:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.7A>G
  hgvsp: ENSP00000418629.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.7A>G
  hgvsp: ENSP00000419594.1:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.7A>G
  hgvsp: ENSP00000375761.3:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.91A>G
  hgvsp: ENSP00000355904.1:p.Asn31Asp
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn31Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-216850817-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850817
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850817
    reference: chr 1
allele count: 1
allele frequency: 8.850810734263259e-6
allele num: 112984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.4T>C
  hgvsp: ENSP00000417900.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.88T>C
  hgvsp: ENSP00000355904.1:p.Ser30Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.4T>C
  hgvsp: ENSP00000352077.2:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.4T>C
  hgvsp: ENSP00000354584.2:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.4T>C
  hgvsp: ENSP00000419594.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.4T>C
  hgvsp: ENSP00000418895.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.4T>C
  hgvsp: ENSP00000375761.3:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.73T>C
  hgvsp: ENSP00000386171.3:p.Ser25Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.4T>C
  hgvsp: ENSP00000355907.2:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.4T>C
  hgvsp: ENSP00000355225.3:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.4T>C
  hgvsp: ENSP00000353108.3:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.4T>C
  hgvsp: ENSP00000420370.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.4T>C
  hgvsp: ENSP00000419155.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.4T>C
  hgvsp: ENSP00000417374.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23950T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.4T>C
  hgvsp: ENSP00000418629.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.4T>C
  hgvsp: ENSP00000355905.2:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.4T>C
  hgvsp: ENSP00000419514.1:p.Ser2Pro
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser30Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

1-216850830-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850830
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850830
    reference: chr 1
allele count: 1
allele frequency: 9.424537726424519e-6
allele num: 106106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.60T>A
  hgvsp: ENST00000408911.3:c.60T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.75T>A
  hgvsp: ENST00000366937.1:c.75T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23937T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-10T>A
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu25Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

1-216850836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850836
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850836
    reference: chr 1
allele count: 1
allele frequency: 1.007516069881315e-5
allele num: 99254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23931C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-3C>T
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.72-3C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/1-216850843-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850843
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850843
    reference: chr 1
allele count: 3
allele frequency: 3.089471082550667e-5
allele num: 97104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23924T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-10T>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-10T>G
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-216850851-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850851
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850851
    reference: chr 1
allele count: 5
allele frequency: 5.413716191342385e-5
allele num: 92358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23916G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-18G>T
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

1-216850854-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850854
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850854
    reference: chr 1
allele count: 1
allele frequency: 1.089846985483238e-5
allele num: 91756
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23913T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-21T>C
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-216850874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850874
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850874
    reference: chr 1
allele count: 2
allele frequency: 2.436290990595917e-5
allele num: 82092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23893C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-41C>T
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21718
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

1-216850874-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216850874
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 216850874
    reference: chr 1
allele count: 2
allele frequency: 2.436290990595917e-5
allele num: 82092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419594
  ensembl transcript: ENST00000493603
  gene symbol: ESRRG
  hgvsc: ENST00000493603.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000354584
  ensembl transcript: ENST00000361395
  gene symbol: ESRRG
  hgvsc: ENST00000361395.2:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000386171
  ensembl transcript: ENST00000408911
  gene symbol: ESRRG
  hgvsc: ENST00000408911.3:c.57-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000375761
  ensembl transcript: ENST00000391890
  gene symbol: ESRRG
  hgvsc: ENST00000391890.3:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000353108
  ensembl transcript: ENST00000360012
  gene symbol: ESRRG
  hgvsc: ENST00000360012.3:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000352077
  ensembl transcript: ENST00000359162
  gene symbol: ESRRG
  hgvsc: ENST00000359162.2:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418629
  ensembl transcript: ENST00000463665
  gene symbol: ESRRG
  hgvsc: ENST00000463665.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355905
  ensembl transcript: ENST00000366938
  gene symbol: ESRRG
  hgvsc: ENST00000366938.2:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000420370
  ensembl transcript: ENST00000459955
  gene symbol: ESRRG
  hgvsc: ENST00000459955.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417900
  ensembl transcript: ENST00000469486
  gene symbol: ESRRG
  hgvsc: ENST00000469486.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000466343
  ensembl transcript: ENST00000586199
  gene symbol: ESRRG
  hgvsc: ENST00000586199.1:c.*12+23893C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355907
  ensembl transcript: ENST00000366940
  gene symbol: ESRRG
  hgvsc: ENST00000366940.2:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419514
  ensembl transcript: ENST00000475275
  gene symbol: ESRRG
  hgvsc: ENST00000475275.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355904
  ensembl transcript: ENST00000366937
  gene symbol: ESRRG
  hgvsc: ENST00000366937.1:c.72-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000419155
  ensembl transcript: ENST00000487276
  gene symbol: ESRRG
  hgvsc: ENST00000487276.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000355225
  ensembl transcript: ENST00000361525
  gene symbol: ESRRG
  hgvsc: ENST00000361525.3:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000417374
  ensembl transcript: ENST00000493748
  gene symbol: ESRRG
  hgvsc: ENST00000493748.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196482
  ensembl protein: ENSP00000418895
  ensembl transcript: ENST00000481543
  gene symbol: ESRRG
  hgvsc: ENST00000481543.1:c.-13-41C>G
  variant of: http://identifiers.org/hgnc/3474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19030
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9096
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 7.75e1
variant carriers: 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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-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

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

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

FS
type: SiteQuality
SIO_000300: 4.5744e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.658494e6

MQRankSum
type: SiteQuality
SIO_000300: -1.158e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.145e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

QD
type: SiteQuality
SIO_000300: 2.85e0

VQSLOD
type: SiteQuality
SIO_000300: -4.012e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeDepth
all individuals: 9151
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45207
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9095
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.987e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

DP
type: SiteQuality
SIO_000300: 1.658486e6

MQ
type: SiteQuality
SIO_000300: 6.073e1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 2.158e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.197e0

VQSLOD
type: SiteQuality
SIO_000300: 7.56e-1

GenotypeDepth
all individuals: 143
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9154
bin: 3.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 29205
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1618
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45214
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9102
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.658674e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.095e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 1.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.507e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: -5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.996e0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 342
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1901
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.306e1

DP
type: SiteQuality
SIO_000300: 1.658599e6

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 9.75e1
variant carriers: 8

GenotypeDepth
all individuals: 19031
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45213
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1618
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.04887770086008e-4
allele num: 66738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.334e0

DP
type: SiteQuality
SIO_000300: 1.659868e6

VQSLOD
type: SiteQuality
SIO_000300: -2.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 1.792e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

QD
type: SiteQuality
SIO_000300: 2.486e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19033
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9159
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9102
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45219
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 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: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.448e0

FS
type: SiteQuality
SIO_000300: 3.481e0

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.658505e6

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeDepth
all individuals: 339
bin: 4.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9162
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45225
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1723
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9102
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
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

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: 10406
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

DP
type: SiteQuality
SIO_000300: 1.65864e6

MQRankSum
type: SiteQuality
SIO_000300: -2.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.299e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e0

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

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9162
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45224
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 9103
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 9.75e1
variant carriers: 5

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

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

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
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: 2.81e-1

FS
type: SiteQuality
SIO_000300: 8.324e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.199e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

DP
type: SiteQuality
SIO_000300: 1.658827e6

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

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 29215
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19027
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1721
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
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

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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.398e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 8.013999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -1.022e0

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.656e0

DP
type: SiteQuality
SIO_000300: 1.658462e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.898e1

GenotypeDepth
all individuals: 29217
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9160
bin: 3.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19026
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1720
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 45225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9104
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

FS
type: SiteQuality
SIO_000300: 2.182e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e0

DP
type: SiteQuality
SIO_000300: 1.658522e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.586e0

VQSLOD
type: SiteQuality
SIO_000300: -4.305e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

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

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29214
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19024
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 9105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 280
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: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.9e0

QD
type: SiteQuality
SIO_000300: 1.324e1

DP
type: SiteQuality
SIO_000300: 1.659022e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

GenotypeDepth
all individuals: 19024
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 496
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1458
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9160
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 0
bin: 7.5e0
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: 9103
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45222
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

DP
type: SiteQuality
SIO_000300: 1.658293e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
SIO_000300: 1.67e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 1.2811e1

VQSLOD
type: SiteQuality
SIO_000300: -1.861e0

GenotypeDepth
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29214
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 112
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
bin: 4.25e1
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: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45216
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
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

FS
type: SiteQuality
SIO_000300: 1.327e0

DP
type: SiteQuality
SIO_000300: 1.658471e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

MQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29212
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19015
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

DP
type: SiteQuality
SIO_000300: 1.658217e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

FS
type: SiteQuality
SIO_000300: 5.692e0

VQSLOD
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.246e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.394e0

QD
type: SiteQuality
SIO_000300: 1.502e1

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19000
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9159
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1461
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45187
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9094
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 908
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.993e1

MQRankSum
type: SiteQuality
SIO_000300: -1.36e0

FS
type: SiteQuality
SIO_000300: 4.942e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.026e0

VQSLOD
type: SiteQuality
SIO_000300: -1.462e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.884e0

QD
type: SiteQuality
SIO_000300: 1.618e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.658467e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1461
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29211
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9159
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45194
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1904
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

DP
type: SiteQuality
SIO_000300: 1.658181e6

FS
type: SiteQuality
SIO_000300: 1.026e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.93e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9160
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 29215
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18992
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9097
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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: 11574
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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.658198e6

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 9.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29218
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9158
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1609
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45194
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9092
bin: 6.75e1
variant carriers: 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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.214e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.87e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.776e1

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.28e-1

DP
type: SiteQuality
SIO_000300: 1.658346e6

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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

GenotypeDepth
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29225
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9155
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 45193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9091
bin: 6.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

FS
type: SiteQuality
SIO_000300: 5.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.663e1

DP
type: SiteQuality
SIO_000300: 1.658203e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.52e-1

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18971
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29223
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 9092
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1895
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.847209734460229e-4
allele num: 66732
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.659533e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18970
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1458
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9153
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29227
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1706
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9090
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1897
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.658187e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

QD
type: SiteQuality
SIO_000300: 1.55e1

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29233
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9155
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1458
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9091
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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: 6612
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

FS
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 1.657993e6

VQSLOD
type: SiteQuality
SIO_000300: -1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.288e0

QD
type: SiteQuality
SIO_000300: 1.213e1

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

GenotypeDepth
all individuals: 9154
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18971
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29234
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 498
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
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: 1898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9093
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45194
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.526e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.49e-1

FS
type: SiteQuality
SIO_000300: 3.339e0

QD
type: SiteQuality
SIO_000300: 1.379e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.657934e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29241
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9153
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18965
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1705
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45195
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9092
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 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: 10406
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: 11572
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: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.283e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.657943e6

GenotypeDepth
all individuals: 18963
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9149
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9094
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 45199
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.658099e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.589e0

QD
type: SiteQuality
SIO_000300: 1.378e1

GenotypeDepth
all individuals: 9150
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29247
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45214
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1702
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: -1.691e2

DP
type: SiteQuality
SIO_000300: 1.657999e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.521e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.928e0

FS
type: SiteQuality
SIO_000300: 3.93104e2

QD
type: SiteQuality
SIO_000300: 8.9e-1

MQ
type: SiteQuality
SIO_000300: 4.517e1

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18965
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29247
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45206
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9093
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.376e-1

QD
type: SiteQuality
SIO_000300: 1.783e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 7.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.435e0

DP
type: SiteQuality
SIO_000300: 1.657995e6

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29250
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18968
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9149
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9090
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1890
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1609
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.606e0

MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

QD
type: SiteQuality
SIO_000300: 1.464e1

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
SIO_000300: 1.658128e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18955
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1463
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9142
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45222
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 9.75e1
variant carriers: 2

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 1.657877e6

QD
type: SiteQuality
SIO_000300: 1.127e1

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 140
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29276
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18950
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45229
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9088
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.39e1

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 1.65772e6

FS
type: SiteQuality
SIO_000300: 1.986e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeDepth
all individuals: 1458
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 29282
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18946
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1697
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 1608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9086
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1881
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45229
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994125756758376e-5
allele num: 66732
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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

FS
type: SiteQuality
SIO_000300: 3.262e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.658039e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 88
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 487
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 114
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 18941
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 29289
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 234
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 142
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1457
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9084
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 1883
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348678295270635e-4
allele num: 66732
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: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.844961240310077e-4
allele num: 16512
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.658666e6

VQSLOD
type: SiteQuality
SIO_000300: 5.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.342e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.81e-1

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9132
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29313
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1460
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18929
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 7.25e1
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: 11572
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.657538e6

QD
type: SiteQuality
SIO_000300: 1.034e1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.467e0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29321
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18928
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 333
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45249
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1882
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.022e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.269e0

MQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.115e1

DP
type: SiteQuality
SIO_000300: 1.657537e6

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9123
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18904
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 29332
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1458
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1876
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9082
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45232
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997781641585227e-5
allele num: 66716
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: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.816e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

DP
type: SiteQuality
SIO_000300: 1.657276e6

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 6.605e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeDepth
all individuals: 165
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1455
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9128
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29331
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 18888
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 41
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 45227
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9069
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495352881213648e-5
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.765904285988853e-4
allele num: 10406
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: 908
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.657578e6

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.231e1

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 230
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9117
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 332
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1453
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 485
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18859
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29352
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99895036737142e-5
allele num: 66690
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 8
allele frequency: 4.84613520717228e-4
allele num: 16508
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

FS
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 1.656917e6

QD
type: SiteQuality
SIO_000300: 1.321e1

MQRankSum
type: SiteQuality
SIO_000300: -8.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

GenotypeDepth
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18851
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 327
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9121
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 29359
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1450
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1671
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 9068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45227
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 3
allele frequency: 3.468208092485549e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.206e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.656623e6

FS
type: SiteQuality
SIO_000300: 4.127e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 9117
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18834
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 29350
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1591
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45207
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
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: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 1.655785e6

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 3.136e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

GenotypeDepth
all individuals: 227
bin: 5.25e1
variant carriers: 15

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 12

GenotypeDepth
all individuals: 160
bin: 5.75e1
variant carriers: 18

GenotypeDepth
all individuals: 1439
bin: 3.75e1
variant carriers: 7

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

GenotypeDepth
all individuals: 47
bin: 8.25e1
variant carriers: 10

GenotypeDepth
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 4.75e1
variant carriers: 15

GenotypeDepth
all individuals: 29351
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18824
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 6.75e1
variant carriers: 22

GenotypeDepth
all individuals: 80
bin: 7.25e1
variant carriers: 14

GenotypeDepth
all individuals: 9115
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 474
bin: 4.25e1
variant carriers: 9

GenotypeDepth
all individuals: 34
bin: 8.75e1
variant carriers: 8

GenotypeDepth
all individuals: 145
bin: 6.25e1
variant carriers: 26

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 11

GenotypeDepth
all individuals: 44
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 45201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1686
bin: 9.75e1
variant carriers: 231

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

GenotypeQuality
all individuals: 601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9063
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 214
allele frequency: 2.056901191849289e-2
allele num: 10404
num of homozygotes: 2

Latino
type: Population
allele count: 14
allele frequency: 1.210444406017638e-3
allele num: 11566
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49985000299994e-5
allele num: 66668
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 5.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 1.65716e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

QD
type: SiteQuality
SIO_000300: 1.224e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeDepth
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18766
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9166
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29425
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1453
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9073
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1473
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.28e-2

DP
type: SiteQuality
SIO_000300: 1.64484e6

VQSLOD
type: SiteQuality
SIO_000300: -1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.06e-1

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

GenotypeDepth
all individuals: 1452
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18736
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9163
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29417
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45185
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 601
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1473
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 1.644269e6

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeDepth
all individuals: 18736
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 475
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9163
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29417
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1452
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 217
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1863
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9068
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1584
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 16448
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.237e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e0

FS
type: SiteQuality
SIO_000300: 3.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 1.644269e6

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

GenotypeDepth
all individuals: 217
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18646
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9184
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1448
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 273
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9049
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.506399086703119e-5
allele num: 66572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

DP
type: SiteQuality
SIO_000300: 1.643811e6

GenotypeDepth
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18614
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9170
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1452
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 29429
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 595
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.884e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.263e1

DP
type: SiteQuality
SIO_000300: 1.643395e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.83e-1

GenotypeDepth
all individuals: 353
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1448
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18379
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29363
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1563
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 588
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1847
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44852
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.150061500615006e-5
allele num: 16260
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.35e1

FS
type: SiteQuality
SIO_000300: 2.702e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 1.638757e6

GenotypeDepth
all individuals: 467
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9120
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18107
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29287
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8969
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507159005275056e-5
allele num: 66350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.155e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.27e0

MQRankSum
type: SiteQuality
SIO_000300: -1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.143e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.143e0

DP
type: SiteQuality
SIO_000300: 1.633745e6

QD
type: SiteQuality
SIO_000300: 9.75e0

GenotypeDepth
all individuals: 200
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9124
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 215
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 472
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 120
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17944
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44167
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8924
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.271165182490907e-5
allele num: 15946
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: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017501508750754e-5
allele num: 66280
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.333506673600277e-4
allele num: 11538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.085e1

FS
type: SiteQuality
SIO_000300: 6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

DP
type: SiteQuality
SIO_000300: 1.630878e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

GenotypeDepth
all individuals: 29137
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 464
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9101
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 633
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17802
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1432
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8906
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43866
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510209012927389e-5
allele num: 66216
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 1.627289e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.243e0

FS
type: SiteQuality
SIO_000300: 1.767e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.641e0

QD
type: SiteQuality
SIO_000300: 1.186e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeDepth
all individuals: 465
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16377
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8887
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1505
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1402
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 28552
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 454
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42076
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.274e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.249e0

DP
type: SiteQuality
SIO_000300: 1.596207e6

GenotypeDepth
all individuals: 1657
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1395
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2086
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16154
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8876
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 454
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28398
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 378
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.590741e6

MQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

FS
type: SiteQuality
SIO_000300: 2.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.277e1

VQSLOD
type: SiteQuality
SIO_000300: -7.228e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

MQ
type: SiteQuality
SIO_000300: 5.88e1

GenotypeDepth
all individuals: 27994
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8741
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2036
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 627
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15613
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1383
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2663
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3997
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40803
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533742331288344e-5
allele num: 65200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 1.5754e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

QD
type: SiteQuality
SIO_000300: 2.58e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3937
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8365
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 447
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14609
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26925
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1327
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 810
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38270
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13694
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.942334460131238e-5
allele num: 10058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64396
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 8.316000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.539e0

QD
type: SiteQuality
SIO_000300: 1.175e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

DP
type: SiteQuality
SIO_000300: 1.536106e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

MQ
type: SiteQuality
SIO_000300: 5.368e1

GenotypeDepth
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 806
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26893
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3948
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 446
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1316
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14662
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8329
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5906
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.313149041977475e-5
allele num: 13674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.649e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.629e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 1.534931e6

MQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 5.858e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.844e0

QD
type: SiteQuality
SIO_000300: 1.623e1

GenotypeDepth
all individuals: 4433
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26431
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3371
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 902
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8183
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1299
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14351
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 447
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.996001599360256e-5
allele num: 10004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64060
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.702e0

DP
type: SiteQuality
SIO_000300: 1.520225e6

FS
type: SiteQuality
SIO_000300: 1.6435e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 5.572e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.49e-1

GenotypeDepth
all individuals: 319
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25680
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3913
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1290
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5236
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7943
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13780
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1069
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.262e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.81e-1

DP
type: SiteQuality
SIO_000300: 1.496195e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 3.993e0

GenotypeDepth
all individuals: 627
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11137
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6318
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1951
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10039
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 424
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 312
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13497
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1411
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60256
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.95e-1

DP
type: SiteQuality
SIO_000300: 1.349612e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.445e1

GenotypeDepth
all individuals: 8468
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3493
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4299
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9435
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14860
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16380
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1598
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.05977108944468e-4
allele num: 9436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56864
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.202e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.083e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

DP
type: SiteQuality
SIO_000300: 1.1737e6

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 401
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1585
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 857
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12413
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3392
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18699
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4230
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4072
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17208
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3691
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.377307761247535e-5
allele num: 55790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.691e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

QD
type: SiteQuality
SIO_000300: 1.54e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.106614e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

GenotypeDepth
all individuals: 739
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2079
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2527
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11346
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22380
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 38
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4983
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 895
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5675
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.345095693779904e-5
allele num: 53504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 9.8818e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.532e0

GenotypeDepth
all individuals: 6041
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7055
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22877
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1913
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6033
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.878922250197287e-5
allele num: 53222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.332e0

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 9.65246e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.566e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

GenotypeDepth
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1122
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2634
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 379
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14618
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3300
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4315
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 662
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7667
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4477
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5500
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5666
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48212
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.347345728914039e-4
allele num: 7422
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.437607820586544e-4
allele num: 6956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5092
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.108e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.4114e5

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

GenotypeDepth
all individuals: 115
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3300
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4315
bin: 2.5e0
variant carriers: 0