8-135649901-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649901
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649901
    reference: chr 8
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.215C>G
  hgvsp: ENSP00000427831.1:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.215C>G
  hgvsp: ENSP00000427879.1:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.65C>G
  hgvsp: ENSP00000429983.1:p.Ser22Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.251C>G
  hgvsp: ENSP00000429091.1:p.Ser84Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.215C>G
  hgvsp: ENSP00000428192.1:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.356C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.215C>G
  hgvsp: ENSP00000428483.1:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.251C>G
  hgvsp: ENSP00000367069.3:p.Ser84Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.215C>G
  hgvsp: ENSP00000394501.2:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.251C>G
  hgvsp: ENSP00000429930.1:p.Ser84Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*233C>G
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser84Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

8-135649909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649909
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649909
    reference: chr 8
allele count: 6
allele frequency: 4.969191015702644e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.207G>A
  hgvsp: ENST00000520214.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.207G>A
  hgvsp: ENST00000520356.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.207G>A
  hgvsp: ENST00000518191.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*225G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.57G>A
  hgvsp: ENST00000522257.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.243G>A
  hgvsp: ENST00000377838.3:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.243G>A
  hgvsp: ENST00000523399.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.207G>A
  hgvsp: ENST00000520727.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.348G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.243G>A
  hgvsp: ENST00000523243.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.207G>A
  hgvsp: ENST00000429442.2:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr81Thr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

8-135649910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649910
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649910
    reference: chr 8
allele count: 8
allele frequency: 6.625697768796276e-5
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.242C>T
  hgvsp: ENSP00000367069.3:p.Thr81Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*224C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.206C>T
  hgvsp: ENSP00000428192.1:p.Thr69Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.347C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.242C>T
  hgvsp: ENSP00000429091.1:p.Thr81Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.206C>T
  hgvsp: ENSP00000427831.1:p.Thr69Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.206C>T
  hgvsp: ENSP00000428483.1:p.Thr69Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.56C>T
  hgvsp: ENSP00000429983.1:p.Thr19Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.242C>T
  hgvsp: ENSP00000429930.1:p.Thr81Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.206C>T
  hgvsp: ENSP00000427879.1:p.Thr69Met
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.206C>T
  hgvsp: ENSP00000394501.2:p.Thr69Met
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr81Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-135649915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649915
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649915
    reference: chr 8
allele count: 103
allele frequency: 8.532847320023196e-4
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.201G>A
  hgvsp: ENST00000520356.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.237G>A
  hgvsp: ENST00000523243.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.342G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.51G>A
  hgvsp: ENST00000522257.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.237G>A
  hgvsp: ENST00000377838.3:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.201G>A
  hgvsp: ENST00000518191.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.237G>A
  hgvsp: ENST00000523399.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.201G>A
  hgvsp: ENST00000429442.2:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.201G>A
  hgvsp: ENST00000520727.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.201G>A
  hgvsp: ENST00000520214.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*219G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 9.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly79Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

8-135649927-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649927
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649927
    reference: chr 8
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.189C>G
  hgvsp: ENST00000520727.1:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.225C>G
  hgvsp: ENST00000523243.1:c.225C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.225C>G
  hgvsp: ENST00000523399.1:c.225C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.189C>G
  hgvsp: ENST00000429442.2:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.189C>G
  hgvsp: ENST00000520356.1:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*207C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.189C>G
  hgvsp: ENST00000520214.1:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.330C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.39C>G
  hgvsp: ENST00000522257.1:c.39C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.189C>G
  hgvsp: ENST00000518191.1:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.225C>G
  hgvsp: ENST00000377838.3:c.225C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly75Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

8-135649929-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649929
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649929
    reference: chr 8
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.223G>A
  hgvsp: ENSP00000429091.1:p.Gly75Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.328G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.187G>A
  hgvsp: ENSP00000427831.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.223G>A
  hgvsp: ENSP00000367069.3:p.Gly75Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.223G>A
  hgvsp: ENSP00000429930.1:p.Gly75Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.187G>A
  hgvsp: ENSP00000394501.2:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.187G>A
  hgvsp: ENSP00000428483.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.187G>A
  hgvsp: ENSP00000427879.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.187G>A
  hgvsp: ENSP00000428192.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.37G>A
  hgvsp: ENSP00000429983.1:p.Gly13Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*205G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly75Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-135649943-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649943
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649943
    reference: chr 8
allele count: 7
allele frequency: 5.816272268013826e-5
allele num: 120352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.209T>C
  hgvsp: ENSP00000429930.1:p.Met70Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.23T>C
  hgvsp: ENSP00000429983.1:p.Met8Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.209T>C
  hgvsp: ENSP00000367069.3:p.Met70Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.209T>C
  hgvsp: ENSP00000429091.1:p.Met70Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.173T>C
  hgvsp: ENSP00000428483.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.314T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.173T>C
  hgvsp: ENSP00000427831.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.173T>C
  hgvsp: ENSP00000394501.2:p.Met58Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*191T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.173T>C
  hgvsp: ENSP00000427879.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.173T>C
  hgvsp: ENSP00000428192.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met70Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-135649946-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649946
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649946
    reference: chr 8
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.170T>G
  hgvsp: ENSP00000428192.1:p.Val57Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.170T>G
  hgvsp: ENSP00000427879.1:p.Val57Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.20T>G
  hgvsp: ENSP00000429983.1:p.Val7Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.206T>G
  hgvsp: ENSP00000429091.1:p.Val69Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.311T>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.206T>G
  hgvsp: ENSP00000367069.3:p.Val69Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.170T>G
  hgvsp: ENSP00000427831.1:p.Val57Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.206T>G
  hgvsp: ENSP00000429930.1:p.Val69Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.170T>G
  hgvsp: ENSP00000394501.2:p.Val57Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.170T>G
  hgvsp: ENSP00000428483.1:p.Val57Gly
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*188T>G
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val69Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-135649952-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649952
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649952
    reference: chr 8
allele count: 1
allele frequency: 8.327920185212944e-6
allele num: 120078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.200T>G
  hgvsp: ENSP00000429091.1:p.Phe67Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.164T>G
  hgvsp: ENSP00000427879.1:p.Phe55Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.164T>G
  hgvsp: ENSP00000428483.1:p.Phe55Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.200T>G
  hgvsp: ENSP00000367069.3:p.Phe67Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.164T>G
  hgvsp: ENSP00000394501.2:p.Phe55Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*182T>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.200T>G
  hgvsp: ENSP00000429930.1:p.Phe67Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.305T>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.164T>G
  hgvsp: ENSP00000427831.1:p.Phe55Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.164T>G
  hgvsp: ENSP00000428192.1:p.Phe55Cys
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.14T>G
  hgvsp: ENSP00000429983.1:p.Phe5Cys
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe67Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP

8-135649961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649961
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649961
    reference: chr 8
allele count: 1
allele frequency: 8.362182864214875e-6
allele num: 119586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-6C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-6C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.197-6C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

8-135649962-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649962
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649962
    reference: chr 8
allele count: 4
allele frequency: 3.345096924183379e-5
allele num: 119578
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-7T>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-7T>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.197-7T>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

8-135649962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649962
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649962
    reference: chr 8
allele count: 1
allele frequency: 8.362742310458446e-6
allele num: 119578
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-7T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-7T>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.197-7T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

8-135649964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649964
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649964
    reference: chr 8
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-9C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-9C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8108
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-135649968-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649968
    reference: chr 8
allele count: 1
allele frequency: 8.381386616601851e-6
allele num: 119312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-13G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-13G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-135649971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649971
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649971
    reference: chr 8
allele count: 1
allele frequency: 8.378577652657685e-6
allele num: 119352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-16C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7703
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

8-135649973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649973
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649973
    reference: chr 8
allele count: 2
allele frequency: 1.677655308940225e-5
allele num: 119214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-18C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-18C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29464
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-135649978-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649978
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649978
    reference: chr 8
allele count: 1
allele frequency: 8.405480373203328e-6
allele num: 118970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-23G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-23G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-135649979-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649979
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649979
    reference: chr 8
allele count: 10
allele frequency: 8.403502579875292e-5
allele num: 118998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-24T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-24T>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

8-135649983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649983
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649983
    reference: chr 8
allele count: 1
allele frequency: 8.418075291265404e-6
allele num: 118792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-28C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-28C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-135649989-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649989
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649989
    reference: chr 8
allele count: 1
allele frequency: 8.452228007302725e-6
allele num: 118312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-34G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-34G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

8-135649989-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649989
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649989
    reference: chr 8
allele count: 2
allele frequency: 1.690445601460545e-5
allele num: 118312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-34G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-34G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-135649990-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649990
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649990
    reference: chr 8
allele count: 61
allele frequency: 5.153332770127566e-4
allele num: 118370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-35C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-35C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-135649996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649996
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649996
    reference: chr 8
allele count: 9
allele frequency: 7.64370158988993e-5
allele num: 117744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-41G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-41G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-135649997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649997
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649997
    reference: chr 8
allele count: 3
allele frequency: 2.551541130843029e-5
allele num: 117576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-42C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-42C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

8-135649999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135649999
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135649999
    reference: chr 8
allele count: 53
allele frequency: 4.510254446430091e-4
allele num: 117510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-44G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-44G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 5.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-135650001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135650001
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135650001
    reference: chr 8
allele count: 1
allele frequency: 8.511942254983741e-6
allele num: 117482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-46C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-46C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

8-135650001-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135650001
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135650001
    reference: chr 8
allele count: 1
allele frequency: 8.511942254983741e-6
allele num: 117482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.11-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-46C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-46C>G
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-135651970-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135651970
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135651970
    reference: chr 8
allele count: 9
allele frequency: 8.351893095768374e-4
allele num: 10776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.10+48T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2015T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2015T>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-135651978-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135651978
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135651978
    reference: chr 8
allele count: 1
allele frequency: 9.285051067780872e-5
allele num: 10770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.10+40G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2023G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2023G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-135652020-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652020
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652020
    reference: chr 8
allele count: 9
allele frequency: 8.397089009143497e-4
allele num: 10718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.8G>T
  hgvsp: ENSP00000429983.1:p.Arg3Leu
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2065G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2065G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg3Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

8-135652020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652020
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652020
    reference: chr 8
allele count: 16
allele frequency: 1.492815823847733e-3
allele num: 10718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.8G>A
  hgvsp: ENSP00000429983.1:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2065G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2065G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg3Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

8-135652021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652021
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652021
    reference: chr 8
allele count: 1
allele frequency: 9.335324869305452e-5
allele num: 10712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.7C>T
  hgvsp: ENSP00000429983.1:p.Arg3Ter
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2066C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2066C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg3Ter
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-135652032-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652032
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652032
    reference: chr 8
allele count: 1
allele frequency: 9.347541596560104e-5
allele num: 10698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2077C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.-5C>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2077C>A
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

8-135652043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652043
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652043
    reference: chr 8
allele count: 14
allele frequency: 1.31307447008066e-3
allele num: 10662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2088C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2088C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

8-135652071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135652071
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135652071
    reference: chr 8
allele count: 1
allele frequency: 9.527439024390244e-5
allele num: 10496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.161-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.197-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.161-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.302-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.161-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429983
  ensembl transcript: ENST00000522257
  gene symbol: ZFAT
  hgvsc: ENST00000522257.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*179-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.161-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.161-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.197-2116C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.197-2116C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-135669761-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669761
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669761
    reference: chr 8
allele count: 1
allele frequency: 8.622473615230737e-6
allele num: 115976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+43C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+43C>G
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9628
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

8-135669764-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669764
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669764
    reference: chr 8
allele count: 1
allele frequency: 8.615342201392239e-6
allele num: 116072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+40C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+40C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12315
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-135669784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669784
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669784
    reference: chr 8
allele count: 20
allele frequency: 1.702852277564921e-4
allele num: 117450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+20G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+20G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21301
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-135669786-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669786
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669787
    reference: chr 8
allele count: 3
allele frequency: 2.554017469479491e-5
allele num: 117462
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+17dupG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+17dupG
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

http://identifiers.org/exac.variant/8-135669786-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669786
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669785
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 117462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+17delG
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+17delG
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9573
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: AC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/8-135669788-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669788
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669788
    reference: chr 8
allele count: 1
allele frequency: 8.495599279573181e-6
allele num: 117708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+16G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+16G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

8-135669788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669788
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669788
    reference: chr 8
allele count: 4
allele frequency: 3.398239711829273e-5
allele num: 117708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+16G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+16G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

8-135669789-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669789
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669789
    reference: chr 8
allele count: 1
allele frequency: 8.468834688346883e-6
allele num: 118080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+15G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+15G>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

8-135669789-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669789
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669789
    reference: chr 8
allele count: 52
allele frequency: 4.403794037940379e-4
allele num: 118080
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+15G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+15G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9575
  bin: 9.75e1
  variant carriers: 52
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-135669790-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669790
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669790
    reference: chr 8
allele count: 12
allele frequency: 1.014799154334038e-4
allele num: 118250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+14G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+14G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32353
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

8-135669790-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669790
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669790
    reference: chr 8
allele count: 1
allele frequency: 8.456659619450317e-6
allele num: 118250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+14G>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+14G>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

8-135669797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669797
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669797
    reference: chr 8
allele count: 1
allele frequency: 8.399126490844953e-6
allele num: 119060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+7G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+7G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
hgvs: c.196+7G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-135669803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669803
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669803
    reference: chr 8
allele count: 1
allele frequency: 8.366240546148183e-6
allele num: 119528
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.196+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.160+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.160+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.196+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.160+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*178+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.160+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.160+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.301+1G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.196+1G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33644
  bin: 6.25e1
  variant carriers: 0
hgvs: c.196+1G>A
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

8-135669805-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669805
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669805
    reference: chr 8
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.195T>C
  hgvsp: ENST00000523243.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.159T>C
  hgvsp: ENST00000429442.2:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.195T>C
  hgvsp: ENST00000523399.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*177T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.159T>C
  hgvsp: ENST00000520214.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.159T>C
  hgvsp: ENST00000520356.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.195T>C
  hgvsp: ENST00000377838.3:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.159T>C
  hgvsp: ENST00000520727.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.300T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.159T>C
  hgvsp: ENST00000518191.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.195T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/8-135669807-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669807
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669807
    reference: chr 8
allele count: 1
allele frequency: 8.348220994106157e-6
allele num: 119786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.157G>T
  hgvsp: ENSP00000427831.1:p.Asp53Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.193G>T
  hgvsp: ENSP00000429930.1:p.Asp65Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.157G>T
  hgvsp: ENSP00000428483.1:p.Asp53Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.193G>T
  hgvsp: ENSP00000429091.1:p.Asp65Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.157G>T
  hgvsp: ENSP00000394501.2:p.Asp53Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.157G>T
  hgvsp: ENSP00000427879.1:p.Asp53Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.298G>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.193G>T
  hgvsp: ENSP00000367069.3:p.Asp65Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.157G>T
  hgvsp: ENSP00000428192.1:p.Asp53Tyr
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*175G>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp65Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

8-135669810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669810
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669810
    reference: chr 8
allele count: 9755
allele frequency: 8.125239467590664e-2
allele num: 120058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.190G>A
  hgvsp: ENSP00000429091.1:p.Gly64Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.295G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.154G>A
  hgvsp: ENSP00000394501.2:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.154G>A
  hgvsp: ENSP00000428483.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.154G>A
  hgvsp: ENSP00000427879.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.154G>A
  hgvsp: ENSP00000428192.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.190G>A
  hgvsp: ENSP00000367069.3:p.Gly64Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.190G>A
  hgvsp: ENSP00000429930.1:p.Gly64Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.154G>A
  hgvsp: ENSP00000427831.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.75e1
  variant carriers: 833
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 9.75e1
  variant carriers: 973
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.75e1
  variant carriers: 802
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 6.25e1
  variant carriers: 906
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 5.25e1
  variant carriers: 871
genotype depth: GenotypeDepth
  all individuals: 21906
  bin: 2.75e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9030
  bin: 2.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 3.25e1
  variant carriers: 351
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 448
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 4.25e1
  variant carriers: 625
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 370
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 622
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 8.75e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.75e1
  variant carriers: 898
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.75e1
  variant carriers: 504
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 2
hgvs: p.Gly64Arg
num of homozygotes: 471
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-135669811-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669811
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669811
    reference: chr 8
allele count: 22
allele frequency: 1.831196936906942e-4
allele num: 120140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*171C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.189C>T
  hgvsp: ENST00000523243.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.189C>T
  hgvsp: ENST00000523399.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.294C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.153C>T
  hgvsp: ENST00000520356.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.153C>T
  hgvsp: ENST00000520727.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.153C>T
  hgvsp: ENST00000518191.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.153C>T
  hgvsp: ENST00000429442.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.189C>T
  hgvsp: ENST00000377838.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.153C>T
  hgvsp: ENST00000520214.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25660
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13899
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10016
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr63Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS

8-135669828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669828
    reference: chr 8
allele count: 10
allele frequency: 8.290774026663129e-5
allele num: 120616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.277C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.136C>T
  hgvsp: ENSP00000428483.1:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*154C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.136C>T
  hgvsp: ENSP00000427879.1:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.172C>T
  hgvsp: ENSP00000429091.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.172C>T
  hgvsp: ENSP00000367069.3:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.172C>T
  hgvsp: ENSP00000429930.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.136C>T
  hgvsp: ENSP00000394501.2:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.136C>T
  hgvsp: ENSP00000427831.1:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.136C>T
  hgvsp: ENSP00000428192.1:p.Pro46Ser
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro58Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

8-135669828-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669828
    reference: chr 8
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.172C>G
  hgvsp: ENSP00000367069.3:p.Pro58Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.172C>G
  hgvsp: ENSP00000429091.1:p.Pro58Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.136C>G
  hgvsp: ENSP00000428192.1:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.136C>G
  hgvsp: ENSP00000427879.1:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*154C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.136C>G
  hgvsp: ENSP00000394501.2:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.136C>G
  hgvsp: ENSP00000427831.1:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.136C>G
  hgvsp: ENSP00000428483.1:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.277C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.172C>G
  hgvsp: ENSP00000429930.1:p.Pro58Ala
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8481
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro58Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

8-135669831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669831
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669831
    reference: chr 8
allele count: 6
allele frequency: 4.973887092762995e-5
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.169C>T
  hgvsp: ENSP00000429091.1:p.Pro57Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.133C>T
  hgvsp: ENSP00000428192.1:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.133C>T
  hgvsp: ENSP00000394501.2:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.169C>T
  hgvsp: ENSP00000429930.1:p.Pro57Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.133C>T
  hgvsp: ENSP00000427879.1:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.133C>T
  hgvsp: ENSP00000427831.1:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*151C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.169C>T
  hgvsp: ENSP00000367069.3:p.Pro57Ser
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.274C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.133C>T
  hgvsp: ENSP00000428483.1:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25937
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro57Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

8-135669848-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669848
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669848
    reference: chr 8
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.152C>G
  hgvsp: ENSP00000367069.3:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.116C>G
  hgvsp: ENSP00000427831.1:p.Pro39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*134C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.116C>G
  hgvsp: ENSP00000427879.1:p.Pro39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.116C>G
  hgvsp: ENSP00000394501.2:p.Pro39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.152C>G
  hgvsp: ENSP00000429930.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.116C>G
  hgvsp: ENSP00000428192.1:p.Pro39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.152C>G
  hgvsp: ENSP00000429091.1:p.Pro51Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.257C>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.116C>G
  hgvsp: ENSP00000428483.1:p.Pro39Arg
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro51Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-135669850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669850
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669850
    reference: chr 8
allele count: 2
allele frequency: 1.656698861847882e-5
allele num: 120722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.150G>A
  hgvsp: ENST00000523243.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.150G>A
  hgvsp: ENST00000523399.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.114G>A
  hgvsp: ENST00000520356.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.255G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.114G>A
  hgvsp: ENST00000520214.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.114G>A
  hgvsp: ENST00000429442.2:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.114G>A
  hgvsp: ENST00000518191.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.114G>A
  hgvsp: ENST00000520727.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.150G>A
  hgvsp: ENST00000377838.3:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*132G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26077
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg50Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

8-135669856-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669856
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669856
    reference: chr 8
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.144C>T
  hgvsp: ENST00000523243.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.108C>T
  hgvsp: ENST00000520727.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.249C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.108C>T
  hgvsp: ENST00000520356.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.144C>T
  hgvsp: ENST00000377838.3:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.108C>T
  hgvsp: ENST00000518191.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.144C>T
  hgvsp: ENST00000523399.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.108C>T
  hgvsp: ENST00000520214.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.108C>T
  hgvsp: ENST00000429442.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro48Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-135669876-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669876
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669876
    reference: chr 8
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.88G>A
  hgvsp: ENSP00000427831.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.88G>A
  hgvsp: ENSP00000428483.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.124G>A
  hgvsp: ENSP00000429930.1:p.Val42Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*106G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.88G>A
  hgvsp: ENSP00000427879.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.229G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.88G>A
  hgvsp: ENSP00000394501.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.124G>A
  hgvsp: ENSP00000429091.1:p.Val42Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.88G>A
  hgvsp: ENSP00000428192.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.124G>A
  hgvsp: ENSP00000367069.3:p.Val42Ile
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val42Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

8-135669880-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669880
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669880
    reference: chr 8
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.120T>C
  hgvsp: ENST00000523399.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.225T>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.84T>C
  hgvsp: ENST00000429442.2:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.84T>C
  hgvsp: ENST00000520356.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.120T>C
  hgvsp: ENST00000523243.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.120T>C
  hgvsp: ENST00000377838.3:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.84T>C
  hgvsp: ENST00000520214.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.84T>C
  hgvsp: ENST00000520727.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.84T>C
  hgvsp: ENST00000518191.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*102T>C
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val40Val
num of homozygotes: 1
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-135669882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669882
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669882
    reference: chr 8
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.82G>A
  hgvsp: ENSP00000428192.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.118G>A
  hgvsp: ENSP00000429930.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.118G>A
  hgvsp: ENSP00000367069.3:p.Val40Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.82G>A
  hgvsp: ENSP00000427831.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.82G>A
  hgvsp: ENSP00000394501.2:p.Val28Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.118G>A
  hgvsp: ENSP00000429091.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*100G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.82G>A
  hgvsp: ENSP00000427879.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.82G>A
  hgvsp: ENSP00000428483.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.223G>A
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val40Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-135669885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669885
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669885
    reference: chr 8
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.115G>A
  hgvsp: ENSP00000429091.1:p.Gly39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.79G>A
  hgvsp: ENSP00000394501.2:p.Gly27Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.115G>A
  hgvsp: ENSP00000367069.3:p.Gly39Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.79G>A
  hgvsp: ENSP00000427831.1:p.Gly27Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.79G>A
  hgvsp: ENSP00000428192.1:p.Gly27Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.79G>A
  hgvsp: ENSP00000428483.1:p.Gly27Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.220G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.79G>A
  hgvsp: ENSP00000427879.1:p.Gly27Arg
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.115G>A
  hgvsp: ENSP00000429930.1:p.Gly39Arg
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8460
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly39Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-135669889-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669889
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669889
    reference: chr 8
allele count: 81
allele frequency: 6.707741230249428e-4
allele num: 120756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.75A>C
  hgvsp: ENSP00000428483.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.111A>C
  hgvsp: ENSP00000429091.1:p.Glu37Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.216A>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.75A>C
  hgvsp: ENSP00000427831.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.111A>C
  hgvsp: ENSP00000367069.3:p.Glu37Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.111A>C
  hgvsp: ENSP00000429930.1:p.Glu37Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.75A>C
  hgvsp: ENSP00000428192.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*93A>C
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.75A>C
  hgvsp: ENSP00000427879.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.75A>C
  hgvsp: ENSP00000394501.2:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13959
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26096
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 9.75e1
  variant carriers: 81
hgvs: p.Glu37Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

8-135669894-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669894
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669894
    reference: chr 8
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.106A>G
  hgvsp: ENSP00000367069.3:p.Met36Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.70A>G
  hgvsp: ENSP00000428483.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.70A>G
  hgvsp: ENSP00000394501.2:p.Met24Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.70A>G
  hgvsp: ENSP00000427879.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.211A>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.70A>G
  hgvsp: ENSP00000427831.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.106A>G
  hgvsp: ENSP00000429091.1:p.Met36Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*88A>G
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.70A>G
  hgvsp: ENSP00000428192.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.106A>G
  hgvsp: ENSP00000429930.1:p.Met36Val
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met36Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

8-135669895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669895
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669895
    reference: chr 8
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.69C>T
  hgvsp: ENST00000520727.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.69C>T
  hgvsp: ENST00000429442.2:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.105C>T
  hgvsp: ENST00000523243.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.69C>T
  hgvsp: ENST00000520214.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.105C>T
  hgvsp: ENST00000523399.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.69C>T
  hgvsp: ENST00000518191.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.69C>T
  hgvsp: ENST00000520356.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.105C>T
  hgvsp: ENST00000377838.3:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.210C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His35His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-135669901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669901
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669901
    reference: chr 8
allele count: 1054
allele frequency: 8.72848932540537e-3
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.63G>A
  hgvsp: ENST00000518191.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.99G>A
  hgvsp: ENST00000523399.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.63G>A
  hgvsp: ENST00000429442.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.204G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.99G>A
  hgvsp: ENST00000523243.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.63G>A
  hgvsp: ENST00000520356.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.63G>A
  hgvsp: ENST00000520727.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*81G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.99G>A
  hgvsp: ENST00000377838.3:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.63G>A
  hgvsp: ENST00000520214.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 26080
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.75e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 4.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 40118
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu33Glu
num of homozygotes: 11
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

8-135669909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669909
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669909
    reference: chr 8
allele count: 38
allele frequency: 3.146893684681253e-4
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.55G>A
  hgvsp: ENSP00000428483.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.55G>A
  hgvsp: ENSP00000427831.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.91G>A
  hgvsp: ENSP00000429091.1:p.Val31Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*73G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.196G>A
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.55G>A
  hgvsp: ENSP00000394501.2:p.Val19Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.55G>A
  hgvsp: ENSP00000427879.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.91G>A
  hgvsp: ENSP00000429930.1:p.Val31Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.91G>A
  hgvsp: ENSP00000367069.3:p.Val31Ile
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.55G>A
  hgvsp: ENSP00000428192.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val31Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

8-135669910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135669910
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 135669910
    reference: chr 8
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000394501
  ensembl transcript: ENST00000429442
  gene symbol: ZFAT
  hgvsc: ENST00000429442.2:c.54C>T
  hgvsp: ENST00000429442.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428483
  ensembl transcript: ENST00000520214
  gene symbol: ZFAT
  hgvsc: ENST00000520214.1:c.54C>T
  hgvsp: ENST00000520214.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000367069
  ensembl transcript: ENST00000377838
  gene symbol: ZFAT
  hgvsc: ENST00000377838.3:c.90C>T
  hgvsp: ENST00000377838.3:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427831
  ensembl transcript: ENST00000520727
  gene symbol: ZFAT
  hgvsc: ENST00000520727.1:c.54C>T
  hgvsp: ENST00000520727.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066827
  ensembl transcript: ENST00000522974
  gene symbol: ZFAT
  hgvsc: ENST00000522974.1:n.195C>T
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429091
  ensembl transcript: ENST00000523399
  gene symbol: ZFAT
  hgvsc: ENST00000523399.1:c.90C>T
  hgvsp: ENST00000523399.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000427879
  ensembl transcript: ENST00000520356
  gene symbol: ZFAT
  hgvsc: ENST00000520356.1:c.54C>T
  hgvsp: ENST00000520356.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000428192
  ensembl transcript: ENST00000518191
  gene symbol: ZFAT
  hgvsc: ENST00000518191.1:c.54C>T
  hgvsp: ENST00000518191.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429930
  ensembl transcript: ENST00000523243
  gene symbol: ZFAT
  hgvsc: ENST00000523243.1:c.90C>T
  hgvsp: ENST00000523243.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000066827
  ensembl protein: ENSP00000429050
  ensembl transcript: ENST00000523924
  gene symbol: ZFAT
  hgvsc: ENST00000523924.1:c.*72C>T
  variant of: http://identifiers.org/hgnc/19899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His30His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-135669924-C-T
type: Variant
allele count: 71
allele frequency: 5.880209368581462e-4
allele num: 120744
alternate allele: T
canonical: true
consequence: missense
filter: PASS
hgvs: p.Glu26Lys
num of homozygotes: 4
reference allele: C

GenotypeDepth
all individuals: 612
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9895
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4092
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29574
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3918
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
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: 900
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.27e-1

DP
type: SiteQuality
SIO_000300: 2.623783e6

MQ
type: SiteQuality
SIO_000300: 5.904e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.047e0

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.424e1

VQSLOD
type: SiteQuality
SIO_000300: -2.209e-1

GenotypeDepth
all individuals: 472
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2335
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9866
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2409
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29574
bin: 9.75e1
variant carriers: 6

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

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

GenotypeQuality
all individuals: 4092
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 5.099959200326398e-4
allele num: 9804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
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: 898
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.623561e6

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.269e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeDepth
all individuals: 8736
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29571
bin: 9.75e1
variant carriers: 8

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

GenotypeQuality
all individuals: 9867
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4182
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493780162465154e-5
allele num: 66722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

DP
type: SiteQuality
SIO_000300: 2.623429e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.261e1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

GenotypeDepth
all individuals: 468
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4175
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4091
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29573
bin: 9.75e1
variant carriers: 103

GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.183137525915688e-4
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 92
allele frequency: 1.379268987436659e-3
allele num: 66702
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.036e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

QD
type: SiteQuality
SIO_000300: 1.043e1

DP
type: SiteQuality
SIO_000300: 2.62702e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

GenotypeDepth
all individuals: 6868
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4101
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4167
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 29507
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3928
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2407
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9764
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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
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InbreedingCoeff
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SIO_000300: 8.0e-4

MQ
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FS
type: SiteQuality
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MQRankSum
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DP
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ReadPosRankSum
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QD
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VQSLOD
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SIO_000300: -1.096e0

ClippingRankSum
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SIO_000300: -1.16e0

GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499655079331754e-5
allele num: 66682
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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SIO_000300: -4.71e-1

FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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QD
type: SiteQuality
SIO_000300: 7.4e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

East Asian
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allele frequency: 8.11500115928588e-4
allele num: 8626
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African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 8.64e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -6.909999999999999e-1

ReadPosRankSum
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SIO_000300: 1.15e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

African
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European (Finnish)
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 8.03e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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African
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South Asian
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Latino
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Other
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ClippingRankSum
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QD
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FS
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MQ
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8624
num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

East Asian
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African
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European (Non-Finnish)
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Other
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Latino
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South Asian
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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MQ
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FS
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BaseQRankSum
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QD
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SIO_000300: 1.565e1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ClippingRankSum
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SIO_000300: -6.8e-1

FS
type: SiteQuality
SIO_000300: 1.101e0

VQSLOD
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SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 3.05e-1

BaseQRankSum
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SIO_000300: -2.478e0

DP
type: SiteQuality
SIO_000300: 2.582848e6

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15468
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

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

VQSLOD
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SIO_000300: 1.76e0

QD
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ClippingRankSum
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SIO_000300: -5.21e-1

InbreedingCoeff
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SIO_000300: 5.2e-3

MQRankSum
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SIO_000300: 1.39e0

ReadPosRankSum
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SIO_000300: 6.05e-1

FS
type: SiteQuality
SIO_000300: 5.305e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 2.57505e6

MQ
type: SiteQuality
SIO_000300: 6.01e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.89e-1

ClippingRankSum
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SIO_000300: 1.78e-1

FS
type: SiteQuality
SIO_000300: 4.614e0

VQSLOD
type: SiteQuality
SIO_000300: -3.251e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

DP
type: SiteQuality
SIO_000300: 2.574335e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.154e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15396
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66350
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.192e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.007e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 2.57008e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15218
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.281e0

BaseQRankSum
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DP
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SIO_000300: 2.561701e6

ClippingRankSum
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MQRankSum
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QD
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MQ
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 10

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

Other
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num of homozygotes: 0

East Asian
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allele count: 10
allele frequency: 1.159554730983302e-3
allele num: 8624
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

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

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

South Asian
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allele count: 0
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num of homozygotes: 0

Other
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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509388395822013e-5
allele num: 66252
num of homozygotes: 0

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

European (Finnish)
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FS
type: SiteQuality
SIO_000300: 1.0061e1

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

DP
type: SiteQuality
SIO_000300: 2.542518e6

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

QD
type: SiteQuality
SIO_000300: 9.82e0

GenotypeQuality
all individuals: 3797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5544
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512493193780628e-5
allele num: 66116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.022076860179886e-4
allele num: 9784
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

DP
type: SiteQuality
SIO_000300: 2.542518e6

QD
type: SiteQuality
SIO_000300: 9.82e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 61

East Asian
type: Population
allele count: 4
allele frequency: 4.641448131817127e-4
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.460207612456747e-4
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14770
num of homozygotes: 0

African
type: Population
allele count: 52
allele frequency: 5.314799672935405e-3
allele num: 9784
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: 1.511761504505049e-5
allele num: 66148
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.541944e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

QD
type: SiteQuality
SIO_000300: 1.374e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.548e0

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

GenotypeQuality
all individuals: 3882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.212011029300367e-4
allele num: 66006
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.527e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

DP
type: SiteQuality
SIO_000300: 2.530051e6

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 818
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031405359524676e-5
allele num: 65976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
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: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.043245527539091e-5
allele num: 14198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.1862e1

DP
type: SiteQuality
SIO_000300: 2.524959e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

VQSLOD
type: SiteQuality
SIO_000300: -1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3162
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 52

GenotypeQuality
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GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.273622942371237e-4
allele num: 65974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 36
allele frequency: 5.446293494704993e-3
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.304147465437788e-3
allele num: 868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.843e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.368e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 1799
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.520176e6

QD
type: SiteQuality
SIO_000300: 1.024e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

FS
type: SiteQuality
SIO_000300: 1.1321e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4062
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14138
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65942
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.520176e6

FS
type: SiteQuality
SIO_000300: 1.1321e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.27e0

VQSLOD
type: SiteQuality
SIO_000300: -1.738e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2068
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GenotypeQuality
all individuals: 256
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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African
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Latino
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European (Finnish)
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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MQ
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VQSLOD
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FS
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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African
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European (Finnish)
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VQSLOD
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FS
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East Asian
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allele frequency: 0.0e0
allele num: 2592
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.26349e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.662e0

MQRankSum
type: SiteQuality
SIO_000300: -1.016e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.23e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.872e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

QD
type: SiteQuality
SIO_000300: 9.42e0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
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: 1.526111772426212e-5
allele num: 65526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.02e-1

DP
type: SiteQuality
SIO_000300: 1.932859e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.02e-1

QD
type: SiteQuality
SIO_000300: 1.629e1

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.215e0

GenotypeQuality
all individuals: 7081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5253668507276e-5
allele num: 65558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.047e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.275e0

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

QD
type: SiteQuality
SIO_000300: 6.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

DP
type: SiteQuality
SIO_000300: 1.93382e6

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 20

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 2257
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GenotypeQuality
all individuals: 368
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.19840131174421e-4
allele num: 9758
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.816504717645402e-4
allele num: 14202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
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: 8
allele frequency: 1.214660957760165e-4
allele num: 65862
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

QD
type: SiteQuality
SIO_000300: 1.271e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

DP
type: SiteQuality
SIO_000300: 1.956812e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1525
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
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: 3
allele frequency: 3.485130111524163e-4
allele num: 8608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.96194e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

QD
type: SiteQuality
SIO_000300: 6.25e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

FS
type: SiteQuality
SIO_000300: 9.385e0

GenotypeQuality
all individuals: 510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14196
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

FS
type: SiteQuality
SIO_000300: 9.385e0

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.96194e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 6.25e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeQuality
all individuals: 9549
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31723
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 3.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 1.516208266367468e-5
allele num: 65954
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

QD
type: SiteQuality
SIO_000300: 1.571e1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 2.699e0

DP
type: SiteQuality
SIO_000300: 1.964612e6

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.39178844815588e-4
allele num: 14370
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032416532734936e-5
allele num: 65954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 9752
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.571e1

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 2.699e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

DP
type: SiteQuality
SIO_000300: 1.964612e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 9575
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 500
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GenotypeQuality
all individuals: 7305
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GenotypeQuality
all individuals: 325
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GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 32095
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GenotypeQuality
all individuals: 735
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GenotypeQuality
all individuals: 138
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GenotypeQuality
all individuals: 1532
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GenotypeQuality
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GenotypeQuality
all individuals: 435
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GenotypeQuality
all individuals: 1476
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variant carriers: 0

GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 1001
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GenotypeQuality
all individuals: 2477
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variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513867021920794e-5
allele num: 66056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
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
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.301e1

DP
type: SiteQuality
SIO_000300: 1.967017e6

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

African
type: Population
allele count: 33
allele frequency: 3.378378378378379e-3
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513867021920794e-5
allele num: 66056
num of homozygotes: 0

Latino
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allele count: 18
allele frequency: 1.559251559251559e-3
allele num: 11544
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.617e0

DP
type: SiteQuality
SIO_000300: 1.967017e6

InbreedingCoeff
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SIO_000300: 1.32e-2

VQSLOD
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ReadPosRankSum
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MQRankSum
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SIO_000300: -9.0e-2

ClippingRankSum
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SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.03950103950104e-3
allele num: 11544
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: 874
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.96804e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

InbreedingCoeff
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ClippingRankSum
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SIO_000300: -3.41e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.55e0

BaseQRankSum
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SIO_000300: -1.623e0

QD
type: SiteQuality
SIO_000300: 1.034e1

MQ
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SIO_000300: 5.96e1

MQRankSum
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SIO_000300: -2.9e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14736
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512813530604218e-5
allele num: 66102
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

DP
type: SiteQuality
SIO_000300: 1.96804e6

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 1.034e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66270
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.524859715516116e-5
allele num: 15326
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.164e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
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SIO_000300: -4.4e-2

MQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.394e-1

BaseQRankSum
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SIO_000300: -1.806e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.979974e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.9e-2

DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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SIO_000300: 1.202e1

FS
type: SiteQuality
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15792
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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African
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Latino
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allele num: 11558
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FS
type: SiteQuality
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 3

Latino
type: Population
allele count: 371
allele frequency: 3.209342560553633e-2
allele num: 11560
num of homozygotes: 5

South Asian
type: Population
allele count: 1072
allele frequency: 6.687461010605115e-2
allele num: 16030
num of homozygotes: 30

European (Non-Finnish)
type: Population
allele count: 6095
allele frequency: 9.15907793105521e-2
allele num: 66546
num of homozygotes: 292

European (Finnish)
type: Population
allele count: 780
allele frequency: 1.179316601149078e-1
allele num: 6614
num of homozygotes: 40

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 70
allele frequency: 7.847533632286996e-2
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 1365
allele frequency: 1.39371043496018e-1
allele num: 9794
num of homozygotes: 104

VQSLOD
type: SiteQuality
SIO_000300: 5.08e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

DP
type: SiteQuality
SIO_000300: 2.159328e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

QD
type: SiteQuality
SIO_000300: 1.437e1

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1358
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4448
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.319085487077535e-4
allele num: 16096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.015235748414821e-5
allele num: 66554
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: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.586e1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.862957e6

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

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

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8481
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 9.75e1
variant carriers: 10

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.471789883268483e-4
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 66664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 1.869204e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.315e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

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

GenotypeQuality
all individuals: 2561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 898
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 1.869204e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

QD
type: SiteQuality
SIO_000300: 1.315e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1348
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39755
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4410
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 8492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.457814661134163e-4
allele num: 11568
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: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.017e0

FS
type: SiteQuality
SIO_000300: 5.958e0

QD
type: SiteQuality
SIO_000300: 1.111e1

MQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 1.869434e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
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variant carriers: 0

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

GenotypeQuality
all individuals: 1345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39904
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4396
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8520
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.855e1

FS
type: SiteQuality
SIO_000300: 2.745e0

DP
type: SiteQuality
SIO_000300: 1.87112e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.033e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 7.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4395
bin: 9.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 39920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2326
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8521
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 9802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 1.871296e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

FS
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e0

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

GenotypeQuality
all individuals: 8512
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
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variant carriers: 0

GenotypeQuality
all individuals: 525
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 1340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4393
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 2324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39972
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.201e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.871314e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 8484
bin: 6.75e1
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: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
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: 8624
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.870793e6

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.09e-1

QD
type: SiteQuality
SIO_000300: 8.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.662e0

FS
type: SiteQuality
SIO_000300: 8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4387
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8484
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 1

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.462e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.395e0

VQSLOD
type: SiteQuality
SIO_000300: -2.006e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.870598e6

QD
type: SiteQuality
SIO_000300: 3.31e1

GenotypeQuality
all individuals: 8479
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40037
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

DP
type: SiteQuality
SIO_000300: 1.870667e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.207e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

GenotypeQuality
all individuals: 4384
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40062
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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

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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.87047e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e0

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.412e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40041
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 75
allele frequency: 7.653061224489796e-3
allele num: 9800
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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.478664192949907e-4
allele num: 8624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.135e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

DP
type: SiteQuality
SIO_000300: 1.871463e6

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40149
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4321
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 1.498486528606108e-5
allele num: 66734
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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.867971e6

FS
type: SiteQuality
SIO_000300: 2.508e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

QD
type: SiteQuality
SIO_000300: 1.105e1

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40166
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4320
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2507
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 9800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.03e-1

DP
type: SiteQuality
SIO_000300: 1.867955e6

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.221e0

QD
type: SiteQuality
SIO_000300: 1.414e1

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4667
bin: 9.75e1
variant carriers: 1042

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
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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: 484
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2452
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 775
allele frequency: 1.161361865371936e-2
allele num: 66732
num of homozygotes: 6

Other
type: Population
allele count: 10
allele frequency: 1.111111111111111e-2
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 118
allele frequency: 1.784094345328092e-2
allele num: 6614
num of homozygotes: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 118
allele frequency: 7.146317829457364e-3
allele num: 16512
num of homozygotes: 1

African
type: Population
allele count: 15
allele frequency: 1.530612244897959e-3
allele num: 9800
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.555478741790529e-3
allele num: 11572
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.895554e6

QD
type: SiteQuality
SIO_000300: 1.331e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.455e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

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

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

GenotypeQuality
all individuals: 8572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3718
bin: 9.75e1
variant carriers: 38

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

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 36
allele frequency: 4.174397031539889e-3
allele num: 8624
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: 9800
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: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.199e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

DP
type: SiteQuality
SIO_000300: 1.850014e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.87e0

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40874
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3683
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2481
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 8583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1292
bin: 8.25e1
variant carriers: 0

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

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

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: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.847994e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.71e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.242e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.602e0