19-57988018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988018
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988018
    reference: chr 19
allele count: 2
allele frequency: 1.701345764499719e-5
allele num: 117554
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.56T>C
  hgvsp: ENSP00000470969.1:p.Ile19Thr
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.283T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.56T>C
  hgvsp: ENSP00000348992.3:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+627T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.56T>C
  hgvsp: ENSP00000415214.2:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.56T>C
  hgvsp: ENSP00000341165.4:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.56T>C
  hgvsp: ENSP00000471079.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+627T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.56T>C
  hgvsp: ENSP00000400754.2:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile19Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-57988022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988022
    reference: chr 19
allele count: 3
allele frequency: 2.560032768419436e-5
allele num: 117186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.52G>A
  hgvsp: ENSP00000400754.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.52G>A
  hgvsp: ENSP00000415214.2:p.Val18Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.52G>A
  hgvsp: ENSP00000471079.1:p.Val18Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+623G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.52G>A
  hgvsp: ENSP00000341165.4:p.Val18Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.52G>A
  hgvsp: ENSP00000348992.3:p.Val18Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+623G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.52G>A
  hgvsp: ENSP00000470969.1:p.Val18Ile
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.279G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val18Ile
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-57988036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988036
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988036
    reference: chr 19
allele count: 1
allele frequency: 8.627978809684043e-6
allele num: 115902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+609C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.38C>T
  hgvsp: ENSP00000348992.3:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.38C>T
  hgvsp: ENSP00000415214.2:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.38C>T
  hgvsp: ENSP00000471079.1:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.38C>T
  hgvsp: ENSP00000341165.4:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.38C>T
  hgvsp: ENSP00000400754.2:p.Pro13Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+609C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.38C>T
  hgvsp: ENSP00000470969.1:p.Pro13Leu
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.265C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39152
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro13Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-57988039-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988039
    reference: chr 19
allele count: 1
allele frequency: 8.640503222907702e-6
allele num: 115734
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.35T>A
  hgvsp: ENSP00000470969.1:p.Val12Asp
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+606T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.35T>A
  hgvsp: ENSP00000471079.1:p.Val12Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+606T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.35T>A
  hgvsp: ENSP00000415214.2:p.Val12Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.35T>A
  hgvsp: ENSP00000348992.3:p.Val12Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.262T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.35T>A
  hgvsp: ENSP00000400754.2:p.Val12Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.35T>A
  hgvsp: ENSP00000341165.4:p.Val12Asp
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val12Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

19-57988040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988040
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988040
    reference: chr 19
allele count: 1
allele frequency: 8.64812508648125e-6
allele num: 115632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34G>A
  hgvsp: ENSP00000348992.3:p.Val12Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34G>A
  hgvsp: ENSP00000470969.1:p.Val12Ile
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+605G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34G>A
  hgvsp: ENSP00000415214.2:p.Val12Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34G>A
  hgvsp: ENSP00000471079.1:p.Val12Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+605G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34G>A
  hgvsp: ENSP00000341165.4:p.Val12Ile
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34G>A
  hgvsp: ENSP00000400754.2:p.Val12Ile
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val12Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

19-57988048-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988048
    reference: chr 19
allele count: 1
allele frequency: 8.7139894386448e-6
allele num: 114758
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-8C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+597C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-8C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+597C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-8C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-8C>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-8C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-8C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-8C>G
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
hgvs: c.34-8C>G
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-57988052-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988052
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988052
    reference: chr 19
allele count: 10
allele frequency: 8.728897889352491e-5
allele num: 114562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+593T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-12T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-12T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+593T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-12T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-12T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-12T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-12T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-12T>C
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

19-57988057-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988057
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988057
    reference: chr 19
allele count: 1
allele frequency: 8.8017321808932e-6
allele num: 113614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+588C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-17C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-17C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+588C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-17C>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

19-57988062-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988062
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988062
    reference: chr 19
allele count: 5
allele frequency: 4.423839184597961e-5
allele num: 113024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-22A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-22A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-22A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+583A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-22A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+583A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-22A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-22A>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-22A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-57988064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988064
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988064
    reference: chr 19
allele count: 7
allele frequency: 6.224767460472727e-5
allele num: 112454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-24G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-24G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+581G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-24G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+581G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-24G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-24G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-24G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-24G>A
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 3.75e1
  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: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-57988065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988065
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988065
    reference: chr 19
allele count: 2
allele frequency: 1.778378474506945e-5
allele num: 112462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-25C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+580C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+580C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-25C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6168
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

19-57988070-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988070
    reference: chr 19
allele count: 9
allele frequency: 8.038728809017668e-5
allele num: 111958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-30T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-30T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-30T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-30T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-30T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+575T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-30T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+575T>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-30T>A
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31129
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

19-57988087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988087
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988087
    reference: chr 19
allele count: 1
allele frequency: 9.065689989665113e-6
allele num: 110306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-47G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-47G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+558G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+558G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-47G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-47G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-47G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-47G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-47G>A
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/19-57988089-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988089
    reference: chr 19
allele count: 1
allele frequency: 9.081497357284268e-6
allele num: 110114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+556G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.34-49G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.34-49G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.261-49G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.34-49G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+556G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.34-49G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.34-49G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.34-49G>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27665
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23515
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

19-57988595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988595
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988595
    reference: chr 19
allele count: 2
allele frequency: 1.658787426391308e-5
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+50C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+50C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+50C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30823
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

19-57988602-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988602
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988602
    reference: chr 19
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+43T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+43T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+43T>C
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40718
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

19-57988611-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988611
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988611
    reference: chr 19
allele count: 1
allele frequency: 8.294900295298451e-6
allele num: 120556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+34C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+34C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+34C>G
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30822
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7158
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-57988612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988612
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988612
    reference: chr 19
allele count: 1
allele frequency: 8.29476268683953e-6
allele num: 120558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+33C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+33C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+33C>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3483
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-57988614-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988614
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988614
    reference: chr 19
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+31G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+31G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+31G>C
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30822
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40720
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

19-57988620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988620
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988620
    reference: chr 19
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+25C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+25C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+25C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+25C>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30822
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-57988633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988633
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988633
    reference: chr 19
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260+12G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33+12G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33+12G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30822
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

19-57988645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988645
    reference: chr 19
allele count: 404
allele frequency: 3.35581619430508e-3
allele num: 120388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.33G>A
  hgvsp: ENST00000600175.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.33G>A
  hgvsp: ENST00000356584.3:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.33G>A
  hgvsp: ENST00000596831.1:c.33G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.33G>A
  hgvsp: ENST00000450712.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.260G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-15G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.33G>A
  hgvsp: ENST00000425074.3:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.33G>A
  hgvsp: ENST00000601768.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.33G>A
  hgvsp: ENST00000343280.4:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30821
  bin: 9.75e1
  variant carriers: 351
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
hgvs: c.33G>A
num of homozygotes: 2
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-57988651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988651
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988651
    reference: chr 19
allele count: 3
allele frequency: 2.497710432103905e-5
allele num: 120110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.27G>A
  hgvsp: ENST00000356584.3:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-21G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.27G>A
  hgvsp: ENST00000601768.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.27G>A
  hgvsp: ENST00000343280.4:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.27G>A
  hgvsp: ENST00000600175.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.254G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.27G>A
  hgvsp: ENST00000425074.3:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.27G>A
  hgvsp: ENST00000596831.1:c.27G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.27G>A
  hgvsp: ENST00000450712.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro9Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

19-57988655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988655
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988655
    reference: chr 19
allele count: 3
allele frequency: 2.501751225858101e-5
allele num: 119916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.23G>A
  hgvsp: ENSP00000471647.1:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-25G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.23G>A
  hgvsp: ENSP00000341165.4:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.23G>A
  hgvsp: ENSP00000348992.3:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.250G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.23G>A
  hgvsp: ENSP00000470969.1:p.Gly8Asp
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.23G>A
  hgvsp: ENSP00000400754.2:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.23G>A
  hgvsp: ENSP00000471079.1:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.23G>A
  hgvsp: ENSP00000415214.2:p.Gly8Asp
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly8Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

19-57988660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988660
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988660
    reference: chr 19
allele count: 1
allele frequency: 8.423464402439436e-6
allele num: 118716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.245G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.18G>A
  hgvsp: ENST00000356584.3:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.18G>A
  hgvsp: ENST00000596831.1:c.18G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.18G>A
  hgvsp: ENST00000601768.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.18G>A
  hgvsp: ENST00000425074.3:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-30G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.18G>A
  hgvsp: ENST00000450712.2:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.18G>A
  hgvsp: ENST00000343280.4:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.18G>A
  hgvsp: ENST00000600175.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro6Pro
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-57988661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988661
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988661
    reference: chr 19
allele count: 3
allele frequency: 2.526954177897574e-5
allele num: 118720
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.17C>T
  hgvsp: ENSP00000341165.4:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.244C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.17C>T
  hgvsp: ENSP00000400754.2:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.17C>T
  hgvsp: ENSP00000470969.1:p.Pro6Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.17C>T
  hgvsp: ENSP00000348992.3:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-31C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.17C>T
  hgvsp: ENSP00000415214.2:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.17C>T
  hgvsp: ENSP00000471079.1:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.17C>T
  hgvsp: ENSP00000471647.1:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30617
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40592
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2959
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro6Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

19-57988662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988662
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988662
    reference: chr 19
allele count: 8
allele frequency: 6.765785423115306e-5
allele num: 118242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-32C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.16C>T
  hgvsp: ENSP00000471079.1:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.16C>T
  hgvsp: ENSP00000348992.3:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.16C>T
  hgvsp: ENSP00000415214.2:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.16C>T
  hgvsp: ENSP00000471647.1:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.16C>T
  hgvsp: ENSP00000400754.2:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.16C>T
  hgvsp: ENSP00000470969.1:p.Pro6Ser
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.243C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.16C>T
  hgvsp: ENSP00000341165.4:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30610
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro6Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-57988666-A-AGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988666
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988669
    reference: chr 19
allele count: 42109
allele frequency: 3.527189573142129e-1
allele num: 119384
alternate allele: AGCC
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.9_11dupGGC
  hgvsp: ENSP00000470969.1:p.Ala4dup
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-39_-37dupGGC
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.9_11dupGGC
  hgvsp: ENSP00000341165.4:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.9_11dupGGC
  hgvsp: ENSP00000471079.1:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.236_238dupGGC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.9_11dupGGC
  hgvsp: ENSP00000400754.2:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.9_11dupGGC
  hgvsp: ENSP00000348992.3:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.9_11dupGGC
  hgvsp: ENSP00000471647.1:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.9_11dupGGC
  hgvsp: ENSP00000415214.2:p.Ala4dup
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 459
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 610
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 5.75e1
  variant carriers: 600
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 6.75e1
  variant carriers: 505
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.75e1
  variant carriers: 678
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.75e1
  variant carriers: 487
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 522
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 8.75e1
  variant carriers: 566
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 7.25e1
  variant carriers: 475
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 338
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 28237
  bin: 9.75e1
  variant carriers: 24177
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 574
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 2.75e1
  variant carriers: 465
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.25e1
  variant carriers: 502
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 5.25e1
  variant carriers: 678
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 8.25e1
  variant carriers: 503
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 6.25e1
  variant carriers: 581
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.25e1
  variant carriers: 630
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 578
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 46
hgvs: p.Ala4dup
num of homozygotes: 8543
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-57988666-AGCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988666
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988663
    reference: chr 19
allele count: 1
allele frequency: 8.376331836762046e-6
allele num: 119384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.9_11delGGC
  hgvsp: ENSP00000471647.1:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.236_238delGGC
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-39_-37delGGC
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.9_11delGGC
  hgvsp: ENSP00000471079.1:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.9_11delGGC
  hgvsp: ENSP00000415214.2:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.9_11delGGC
  hgvsp: ENSP00000341165.4:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.9_11delGGC
  hgvsp: ENSP00000348992.3:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.9_11delGGC
  hgvsp: ENSP00000400754.2:p.Ala4del
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.9_11delGGC
  hgvsp: ENSP00000470969.1:p.Ala4del
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28237
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52662
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala4del
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: AGCC
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

19-57988672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988672
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988672
    reference: chr 19
allele count: 6
allele frequency: 4.984465083822088e-5
allele num: 120374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.6G>A
  hgvsp: ENST00000601768.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.6G>A
  hgvsp: ENST00000600175.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-42G>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.233G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.6G>A
  hgvsp: ENST00000343280.4:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.6G>A
  hgvsp: ENST00000596831.1:c.6G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.6G>A
  hgvsp: ENST00000425074.3:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.6G>A
  hgvsp: ENST00000356584.3:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.6G>A
  hgvsp: ENST00000450712.2:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala2Ala
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-57988681-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988681
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988681
    reference: chr 19
allele count: 1
allele frequency: 8.320021299254527e-6
allele num: 120192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-51C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-4C>A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-4C>A
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.224C>A
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

19-57988684-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988684
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988684
    reference: chr 19
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-7A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-54A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.221A>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-7A>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6091
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-57988685-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988685
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988684
    reference: chr 19
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-56delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-9delA
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.219delA
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-9delA
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: GT
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-57988688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988688
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988688
    reference: chr 19
allele count: 6
allele frequency: 4.982974835977079e-5
allele num: 120410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-58C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-11C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.217C>T
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-57988691-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988691
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988692
    reference: chr 19
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-15dupT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-15dupT
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.213dupT
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-62dupT
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6021
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-57988694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988694
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988694
    reference: chr 19
allele count: 7
allele frequency: 5.813663770908426e-5
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-17C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-64C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-17C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.211C>T
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-57988698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988698
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988698
    reference: chr 19
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.207C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-21C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-68C>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/19-57988704-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988704
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988704
    reference: chr 19
allele count: 2
allele frequency: 1.661157162079104e-5
allele num: 120398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.201G>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-27G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-74G>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-27G>T
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5905
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-57988705-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988705
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988705
    reference: chr 19
allele count: 3
allele frequency: 2.491321895397698e-5
allele num: 120418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-75C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-28C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.200C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-28C>G
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

19-57988710-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988710
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988710
    reference: chr 19
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.195C>G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-33C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-80C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-33C>G
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-57988711-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988711
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988711
    reference: chr 19
allele count: 7
allele frequency: 5.813470641973258e-5
allele num: 120410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-81A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-34A>T
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-34A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.194A>T
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5197
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD

19-57988711-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988711
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988711
    reference: chr 19
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-34A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.194A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-34A>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-81A>C
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

19-57988718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988718
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988718
    reference: chr 19
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-88T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-41T>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-41T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.187T>C
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

19-57988728-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57988728
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57988728
    reference: chr 19
allele count: 1548
allele frequency: 1.287939297124601e-2
allele num: 120192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471647
  ensembl transcript: ENST00000601768
  gene symbol: ZNF772
  hgvsc: ENST00000601768.1:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268163
  ensembl protein: ENSP00000470969
  ensembl transcript: ENST00000596831
  gene symbol: AC004076.9
  hgvsc: ENST00000596831.1:c.-51T>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000415214
  ensembl transcript: ENST00000425074
  gene symbol: ZNF772
  hgvsc: ENST00000425074.3:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000400754
  ensembl transcript: ENST00000450712
  gene symbol: ZNF772
  hgvsc: ENST00000450712.2:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000268163
  ensembl transcript: ENST00000415705
  gene symbol: AC004076.9
  hgvsc: ENST00000415705.3:n.177T>C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000341165
  ensembl transcript: ENST00000343280
  gene symbol: ZNF772
  hgvsc: ENST00000343280.4:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000348992
  ensembl transcript: ENST00000356584
  gene symbol: ZNF772
  hgvsc: ENST00000356584.3:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000395967
  ensembl transcript: ENST00000427512
  gene symbol: ZNF772
  hgvsc: ENST00000427512.2:c.-98T>C
  variant of: http://identifiers.org/hgnc/33106
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197128
  ensembl protein: ENSP00000471079
  ensembl transcript: ENST00000600175
  gene symbol: ZNF772
  hgvsc: ENST00000600175.1:c.-51T>C
  variant of: http://identifiers.org/hgnc/33106
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 5.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 9.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 7.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 2.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 3.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 3.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 4.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 9.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 6.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 8.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 7.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 8.25e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 54
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

19-57999278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999278
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999278
    reference: chr 19
allele count: 2
allele frequency: 1.686653510769283e-5
allele num: 118578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-41C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-41C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.191C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-225C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-41C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12038
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10584
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

19-57999279-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999279
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999279
    reference: chr 19
allele count: 1
allele frequency: 8.432840855427377e-6
allele num: 118584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-40T>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-40T>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-224T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.192T>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-40T>A
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

19-57999280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999280
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999280
    reference: chr 19
allele count: 1
allele frequency: 8.432129787341686e-6
allele num: 118594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-223C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-39C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-39C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.193C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

19-57999285-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999285
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999285
    reference: chr 19
allele count: 1
allele frequency: 8.424741781664392e-6
allele num: 118698
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.198A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-34A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-218A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-34A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-34A>G
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-57999288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999288
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999288
    reference: chr 19
allele count: 1
allele frequency: 8.422329279385507e-6
allele num: 118732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-31G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.201G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-31G>A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-31G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-215G>A
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

19-57999290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999290
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999290
    reference: chr 19
allele count: 2
allele frequency: 1.683671751355356e-5
allele num: 118788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.203C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-29C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-29C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-213C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-57999293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999293
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999293
    reference: chr 19
allele count: 1
allele frequency: 8.41651657212113e-6
allele num: 118814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-26C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.206C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-26C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-26C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-210C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

19-57999294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999294
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999294
    reference: chr 19
allele count: 1
allele frequency: 8.413259296651523e-6
allele num: 118860
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-25C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-25C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.207C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-209C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-25C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

19-57999297-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999297
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999297
    reference: chr 19
allele count: 1
allele frequency: 8.409863087428936e-6
allele num: 118908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.210C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-22C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-22C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-206C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-22C>G
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

19-57999299-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999299
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999299
    reference: chr 19
allele count: 1
allele frequency: 8.410428931875526e-6
allele num: 118900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.212A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-20A>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-204A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-20A>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-57999303-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999303
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999303
    reference: chr 19
allele count: 1
allele frequency: 8.409297319116015e-6
allele num: 118916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-200C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-16C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.216C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-16C>G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-16C>G
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-57999308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999308
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999308
    reference: chr 19
allele count: 1
allele frequency: 8.418500496691529e-6
allele num: 118786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-195C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-11C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-11C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.221C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

19-57999309-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999309
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999309
    reference: chr 19
allele count: 1
allele frequency: 8.423464402439436e-6
allele num: 118716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.222A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-10A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-194A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-10A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

19-57999312-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999312
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999312
    reference: chr 19
allele count: 1
allele frequency: 8.437109783672505e-6
allele num: 118524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.225G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-7G>T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-7G>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-191G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-7G>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

19-57999313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999313
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999313
    reference: chr 19
allele count: 6
allele frequency: 5.062265870203503e-5
allele num: 118524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.-6G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.226G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.-6G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-190G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

19-57999331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999331
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999331
    reference: chr 19
allele count: 1
allele frequency: 8.477881207928515e-6
allele num: 117954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.13G>A
  hgvsp: ENSP00000392129.2:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.13G>A
  hgvsp: ENSP00000414709.2:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.13G>A
  hgvsp: ENSP00000299860.9:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.244G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.13G>A
  hgvsp: ENSP00000429471.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.13G>A
  hgvsp: ENSP00000390916.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.13G>A
  hgvsp: ENSP00000427723.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.13G>A
  hgvsp: ENSP00000428523.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.13G>A
  hgvsp: ENSP00000472846.1:p.Ala5Thr
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-172G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.13G>A
  hgvsp: ENSP00000428181.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.13G>A
  hgvsp: ENSP00000429504.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.13G>A
  hgvsp: ENSP00000388864.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.13G>A
  hgvsp: ENSP00000428515.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.13G>A
  hgvsp: ENSP00000429628.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.13G>A
  hgvsp: ENSP00000346136.4:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.13G>A
  hgvsp: ENSP00000221735.7:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.13G>A
  hgvsp: ENSP00000471625.1:p.Ala5Thr
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala5Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

19-57999332-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999332
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999332
    reference: chr 19
allele count: 2
allele frequency: 1.695835029168363e-5
allele num: 117936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-171C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.14C>T
  hgvsp: ENSP00000429504.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.14C>T
  hgvsp: ENSP00000428523.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.14C>T
  hgvsp: ENSP00000221735.7:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.14C>T
  hgvsp: ENSP00000427723.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.14C>T
  hgvsp: ENSP00000428181.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.14C>T
  hgvsp: ENSP00000414709.2:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.14C>T
  hgvsp: ENSP00000429471.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.14C>T
  hgvsp: ENSP00000299860.9:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.14C>T
  hgvsp: ENSP00000388864.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.14C>T
  hgvsp: ENSP00000472846.1:p.Ala5Val
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.14C>T
  hgvsp: ENSP00000428515.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.14C>T
  hgvsp: ENSP00000429628.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.14C>T
  hgvsp: ENSP00000471625.1:p.Ala5Val
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.14C>T
  hgvsp: ENSP00000346136.4:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.14C>T
  hgvsp: ENSP00000390916.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.245C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.14C>T
  hgvsp: ENSP00000392129.2:p.Ala5Val
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala5Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-57999333-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999333
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999333
    reference: chr 19
allele count: 409
allele frequency: 3.467629802964018e-3
allele num: 117948
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.15C>G
  hgvsp: ENST00000601674.1:c.15C>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.15C>G
  hgvsp: ENST00000520540.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.15C>G
  hgvsp: ENST00000221735.7:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.15C>G
  hgvsp: ENST00000599674.1:c.15C>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.15C>G
  hgvsp: ENST00000442920.2:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.15C>G
  hgvsp: ENST00000521137.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.15C>G
  hgvsp: ENST00000426954.2:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.15C>G
  hgvsp: ENST00000347466.6:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.15C>G
  hgvsp: ENST00000521754.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.15C>G
  hgvsp: ENST00000415379.2:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.15C>G
  hgvsp: ENST00000523138.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.15C>G
  hgvsp: ENST00000354197.4:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.15C>G
  hgvsp: ENST00000518999.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.246C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.15C>G
  hgvsp: ENST00000424930.2:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-170C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.15C>G
  hgvsp: ENST00000523312.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.1C>G
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.15C>G
  hgvsp: ENST00000523882.1:c.15C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala5Ala
num of homozygotes: 7
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

19-57999333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999333
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999333
    reference: chr 19
allele count: 4
allele frequency: 3.391324990673856e-5
allele num: 117948
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.15C>T
  hgvsp: ENST00000424930.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.15C>T
  hgvsp: ENST00000523138.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-170C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.15C>T
  hgvsp: ENST00000347466.6:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.15C>T
  hgvsp: ENST00000521137.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.15C>T
  hgvsp: ENST00000415379.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.15C>T
  hgvsp: ENST00000520540.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.15C>T
  hgvsp: ENST00000599674.1:c.15C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.15C>T
  hgvsp: ENST00000523312.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.15C>T
  hgvsp: ENST00000426954.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.15C>T
  hgvsp: ENST00000518999.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.15C>T
  hgvsp: ENST00000442920.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.15C>T
  hgvsp: ENST00000601674.1:c.15C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.15C>T
  hgvsp: ENST00000221735.7:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.15C>T
  hgvsp: ENST00000521754.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.15C>T
  hgvsp: ENST00000354197.4:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.15C>T
  hgvsp: ENST00000523882.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.1C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.246C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala5Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

19-57999334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999334
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999334
    reference: chr 19
allele count: 1
allele frequency: 8.47860001356576e-6
allele num: 117944
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.16C>T
  hgvsp: ENST00000424930.2:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.16C>T
  hgvsp: ENST00000347466.6:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-169C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.16C>T
  hgvsp: ENST00000521137.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.16C>T
  hgvsp: ENST00000426954.2:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.16C>T
  hgvsp: ENST00000523138.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.16C>T
  hgvsp: ENST00000599674.1:c.16C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.16C>T
  hgvsp: ENST00000521754.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.2C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.16C>T
  hgvsp: ENST00000221735.7:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.16C>T
  hgvsp: ENST00000415379.2:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.16C>T
  hgvsp: ENST00000520540.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.16C>T
  hgvsp: ENST00000601674.1:c.16C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.16C>T
  hgvsp: ENST00000354197.4:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.16C>T
  hgvsp: ENST00000442920.2:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.16C>T
  hgvsp: ENST00000518999.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.16C>T
  hgvsp: ENST00000523882.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.16C>T
  hgvsp: ENST00000523312.1:c.16C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.247C>T
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu6Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-57999340-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999340
    reference: chr 19
allele count: 5
allele frequency: 4.245347099578862e-5
allele num: 117776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.22G>A
  hgvsp: ENSP00000428515.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.22G>A
  hgvsp: ENSP00000392129.2:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.22G>A
  hgvsp: ENSP00000390916.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.22G>A
  hgvsp: ENSP00000472846.1:p.Asp8Asn
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.22G>A
  hgvsp: ENSP00000429471.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.22G>A
  hgvsp: ENSP00000221735.7:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.253G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.22G>A
  hgvsp: ENSP00000429504.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.22G>A
  hgvsp: ENSP00000414709.2:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.22G>A
  hgvsp: ENSP00000429628.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.22G>A
  hgvsp: ENSP00000346136.4:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.22G>A
  hgvsp: ENSP00000427723.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.22G>A
  hgvsp: ENSP00000388864.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.22G>A
  hgvsp: ENSP00000299860.9:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.22G>A
  hgvsp: ENSP00000428523.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.22G>A
  hgvsp: ENSP00000471625.1:p.Asp8Asn
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.22G>A
  hgvsp: ENSP00000428181.1:p.Asp8Asn
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.8G>A
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp8Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-57999343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999343
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999343
    reference: chr 19
allele count: 45
allele frequency: 3.821980635298114e-4
allele num: 117740
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.25C>T
  hgvsp: ENSP00000388864.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.25C>T
  hgvsp: ENSP00000428523.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.25C>T
  hgvsp: ENSP00000429504.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.25C>T
  hgvsp: ENSP00000471625.1:p.Pro9Ser
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.25C>T
  hgvsp: ENSP00000221735.7:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.25C>T
  hgvsp: ENSP00000390916.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.25C>T
  hgvsp: ENSP00000429628.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.11C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.25C>T
  hgvsp: ENSP00000428515.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.256C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.25C>T
  hgvsp: ENSP00000299860.9:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.25C>T
  hgvsp: ENSP00000429471.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.25C>T
  hgvsp: ENSP00000427723.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.25C>T
  hgvsp: ENSP00000414709.2:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.25C>T
  hgvsp: ENSP00000472846.1:p.Pro9Ser
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.25C>T
  hgvsp: ENSP00000428181.1:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.25C>T
  hgvsp: ENSP00000392129.2:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-160C>T
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.25C>T
  hgvsp: ENSP00000346136.4:p.Pro9Ser
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro9Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-57999344-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57999344
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 57999344
    reference: chr 19
allele count: 2
allele frequency: 1.698831204131557e-5
allele num: 117728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429471
  ensembl transcript: ENST00000520540
  gene symbol: ZNF419
  hgvsc: ENST00000520540.1:c.26C>A
  hgvsp: ENSP00000429471.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428515
  ensembl transcript: ENST00000523312
  gene symbol: ZNF419
  hgvsc: ENST00000523312.1:c.26C>A
  hgvsp: ENSP00000428515.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000472846
  ensembl transcript: ENST00000599674
  gene symbol: AC003005.4
  hgvsc: ENST00000599674.1:c.26C>A
  hgvsp: ENSP00000472846.1:p.Pro9His
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000346136
  ensembl transcript: ENST00000354197
  gene symbol: ZNF419
  hgvsc: ENST00000354197.4:c.26C>A
  hgvsp: ENSP00000346136.4:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428523
  ensembl transcript: ENST00000521754
  gene symbol: ZNF419
  hgvsc: ENST00000521754.1:c.26C>A
  hgvsp: ENSP00000428523.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429504
  ensembl transcript: ENST00000523138
  gene symbol: ZNF419
  hgvsc: ENST00000523138.1:c.26C>A
  hgvsp: ENSP00000429504.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429628
  ensembl transcript: ENST00000521137
  gene symbol: ZNF419
  hgvsc: ENST00000521137.1:c.26C>A
  hgvsp: ENSP00000429628.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000428181
  ensembl transcript: ENST00000523882
  gene symbol: ZNF419
  hgvsc: ENST00000523882.1:c.26C>A
  hgvsp: ENSP00000428181.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000388864
  ensembl transcript: ENST00000424930
  gene symbol: ZNF419
  hgvsc: ENST00000424930.2:c.26C>A
  hgvsp: ENSP00000388864.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000523439
  gene symbol: ZNF419
  hgvsc: ENST00000523439.1:n.257C>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105136
  ensembl transcript: ENST00000522346
  gene symbol: ZNF419
  hgvsc: ENST00000522346.1:n.12C>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000427723
  ensembl transcript: ENST00000518999
  gene symbol: ZNF419
  hgvsc: ENST00000518999.1:c.26C>A
  hgvsp: ENSP00000427723.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000414709
  ensembl transcript: ENST00000442920
  gene symbol: ZNF419
  hgvsc: ENST00000442920.2:c.26C>A
  hgvsp: ENSP00000414709.2:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000392129
  ensembl transcript: ENST00000415379
  gene symbol: ZNF419
  hgvsc: ENST00000415379.2:c.26C>A
  hgvsp: ENSP00000392129.2:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000390916
  ensembl transcript: ENST00000426954
  gene symbol: ZNF419
  hgvsc: ENST00000426954.2:c.26C>A
  hgvsp: ENSP00000390916.1:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000429880
  ensembl transcript: ENST00000519310
  gene symbol: ZNF419
  hgvsc: ENST00000519310.1:c.-159C>A
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000268107
  ensembl protein: ENSP00000471625
  ensembl transcript: ENST00000601674
  gene symbol: AC003005.4
  hgvsc: ENST00000601674.1:c.26C>A
  hgvsp: ENSP00000471625.1:p.Pro9His
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000221735
  ensembl transcript: ENST00000221735
  gene symbol: ZNF419
  hgvsc: ENST00000221735.7:c.26C>A
  hgvsp: ENSP00000221735.7:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105136
  ensembl protein: ENSP00000299860
  ensembl transcript: ENST00000347466
  gene symbol: ZNF419
  hgvsc: ENST00000347466.6:c.26C>A
  hgvsp: ENSP00000299860.9:p.Pro9His
  variant of: http://identifiers.org/hgnc/20648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Pro9His
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 3130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40218
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 322
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6579
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0269e1

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.474879e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.842e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39938
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2246
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13862
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: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.92169848071679e-4
allele num: 10268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

FS
type: SiteQuality
SIO_000300: 1.724e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.09e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

DP
type: SiteQuality
SIO_000300: 1.470112e6

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4015
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65122
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13002
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

FS
type: SiteQuality
SIO_000300: 5.202e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.095e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.035e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.453109e6

QD
type: SiteQuality
SIO_000300: 5.89e0

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2060
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4092
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.765180928715639e-5
allele num: 12878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
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: 6588
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 1.666e1

DP
type: SiteQuality
SIO_000300: 1.450501e6

VQSLOD
type: SiteQuality
SIO_000300: -2.167e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.456e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.643e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 7.5e0
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65072
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.232e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 1.450564e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.066e0

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6388
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 9.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.096e0

DP
type: SiteQuality
SIO_000300: 1.440329e6

FS
type: SiteQuality
SIO_000300: 4.301e0

MQ
type: SiteQuality
SIO_000300: 5.758e1

VQSLOD
type: SiteQuality
SIO_000300: -2.08e0

QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
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allele count: 10
allele frequency: 1.543066999969139e-4
allele num: 64806
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12062
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
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SIO_000300: -1.8e-2

MQRankSum
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SIO_000300: 1.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.81e-1

DP
type: SiteQuality
SIO_000300: 1.437746e6

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
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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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bin: 3.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64572
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 8.76731544800982e-5
allele num: 11406
num of homozygotes: 0

East Asian
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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: 6576
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 2.405e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.42774e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.146e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11000
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African
type: Population
allele count: 4
allele frequency: 3.933910306845004e-4
allele num: 10168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64440
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.306e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.758e0

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.420079e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 1.307e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-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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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.394964299135663e-5
allele num: 10644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.777017358302744e-5
allele num: 64292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

DP
type: SiteQuality
SIO_000300: 1.419325e6

QD
type: SiteQuality
SIO_000300: 1.022e1

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.458e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555161581288296e-5
allele num: 64302
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.745845723281441e-5
allele num: 11434
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8564
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10624
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 1.0979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.883e1

MQRankSum
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DP
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8554
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele 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
allele num: 64170
num of homozygotes: 0

Other
type: Population
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South Asian
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allele frequency: 8.7497569511958e-4
allele num: 10286
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.581e0

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 3.22e-1

InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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African
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.569119723834929e-5
allele num: 63730
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ClippingRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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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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East Asian
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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: 6534
num of homozygotes: 0

African
type: Population
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Latino
type: Population
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Other
type: Population
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.571240022625856e-5
allele num: 63644
num of homozygotes: 0

South Asian
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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FS
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.046e0

VQSLOD
type: SiteQuality
SIO_000300: -1.263e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.018867924528302e-5
allele num: 66250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.31e0

MQ
type: SiteQuality
SIO_000300: 5.87e1

DP
type: SiteQuality
SIO_000300: 7.17699e6

FS
type: SiteQuality
SIO_000300: 4.842e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.065e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

GenotypeQuality
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bin: 9.25e1
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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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1706
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

DP
type: SiteQuality
SIO_000300: 7.179141e6

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

FS
type: SiteQuality
SIO_000300: 1.436e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
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: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.181777e6

FS
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.965e0

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 44
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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
all individuals: 96
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GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 10236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.312e0

FS
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.085e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

QD
type: SiteQuality
SIO_000300: 1.429e1

DP
type: SiteQuality
SIO_000300: 7.18206e6

GenotypeQuality
all individuals: 70
bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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: 1
allele frequency: 6.112469437652811e-5
allele num: 16360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.524e0

FS
type: SiteQuality
SIO_000300: 4.317e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 7.182621e6

VQSLOD
type: SiteQuality
SIO_000300: -6.229e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.382e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

QD
type: SiteQuality
SIO_000300: 1.484e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.184402e6

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.92e-1

MQ
type: SiteQuality
SIO_000300: 5.761e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.21e-1

FS
type: SiteQuality
SIO_000300: 9.865e0

QD
type: SiteQuality
SIO_000300: 1.208e1

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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bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.811616954474098e-5
allele num: 10192
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.728e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 7.185491e6

FS
type: SiteQuality
SIO_000300: 6.469e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.924e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

QD
type: SiteQuality
SIO_000300: 1.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-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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variant carriers: 401

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1332
bin: 9.25e1
variant carriers: 1

Latino
type: Population
allele count: 6
allele frequency: 5.184929139301763e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.432794063982484e-4
allele num: 16442
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.941688080648349e-4
allele num: 10118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 370
allele frequency: 5.596732718196945e-3
allele num: 66110
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 19
allele frequency: 2.872694284850318e-3
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

DP
type: SiteQuality
SIO_000300: 7.185899e6

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.581e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 273
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GenotypeQuality
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GenotypeQuality
all individuals: 237
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 71
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GenotypeQuality
all individuals: 2194
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
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: 3
allele frequency: 4.548900682335102e-5
allele num: 65950
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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.661e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

QD
type: SiteQuality
SIO_000300: 1.178e1

DP
type: SiteQuality
SIO_000300: 7.13743e6

FS
type: SiteQuality
SIO_000300: 3.424e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.519e0

VQSLOD
type: SiteQuality
SIO_000300: -3.784e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 65870
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.005409737527549e-4
allele num: 9982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

DP
type: SiteQuality
SIO_000300: 7.142992e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 1.3672e1

VQSLOD
type: SiteQuality
SIO_000300: -9.596e-1

MQ
type: SiteQuality
SIO_000300: 5.652e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.2758880381574e-5
allele num: 15934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.644e0

FS
type: SiteQuality
SIO_000300: 4.026e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.72e-1

QD
type: SiteQuality
SIO_000300: 1.967e1

MQ
type: SiteQuality
SIO_000300: 5.753e1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 7.142487e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1303
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.065603923973023e-4
allele num: 9786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65450
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.3e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 1.214e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.351e1

DP
type: SiteQuality
SIO_000300: 7.142425e6

GenotypeQuality
all individuals: 232
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40591
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 7.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 65298
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.084530316512013e-4
allele num: 15734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.140113e6

FS
type: SiteQuality
SIO_000300: 5.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.556e0

GenotypeQuality
all individuals: 676
bin: 9.25e1
variant carriers: 69

GenotypeQuality
all individuals: 708
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variant carriers: 68

GenotypeQuality
all individuals: 950
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GenotypeQuality
all individuals: 80
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variant carriers: 28

GenotypeQuality
all individuals: 171
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variant carriers: 30

GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 115
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 68

GenotypeQuality
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GenotypeQuality
all individuals: 52662
bin: 9.75e1
variant carriers: 33125

European (Finnish)
type: Population
allele count: 2251
allele frequency: 3.411639890876023e-1
allele num: 6598
num of homozygotes: 393

South Asian
type: Population
allele count: 7201
allele frequency: 4.371661000485673e-1
allele num: 16472
num of homozygotes: 1691

European (Non-Finnish)
type: Population
allele count: 17535
allele frequency: 2.675955316811134e-1
allele num: 65528
num of homozygotes: 2382

Other
type: Population
allele count: 286
allele frequency: 3.19910514541387e-1
allele num: 894
num of homozygotes: 44

African
type: Population
allele count: 3028
allele frequency: 3.104367438999385e-1
allele num: 9754
num of homozygotes: 466

Latino
type: Population
allele count: 6377
allele frequency: 5.531748785565579e-1
allele num: 11528
num of homozygotes: 1863

East Asian
type: Population
allele count: 5431
allele frequency: 6.307781649245063e-1
allele num: 8610
num of homozygotes: 1704

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

QD
type: SiteQuality
SIO_000300: 2.429e1

MQ
type: SiteQuality
SIO_000300: 5.756e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

DP
type: SiteQuality
SIO_000300: 5.995457e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.829999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526065193505067e-5
allele num: 65528
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

MQRankSum
type: SiteQuality
SIO_000300: -9.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

MQ
type: SiteQuality
SIO_000300: 5.756e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

DP
type: SiteQuality
SIO_000300: 5.995457e6

QD
type: SiteQuality
SIO_000300: 2.429e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.829999999999999e-2

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 1
allele frequency: 9.936406995230525e-5
allele num: 10064
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.049789769805499e-5
allele num: 66118
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.855e0

FS
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.398e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 3.909192e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43622
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1645
bin: 7.75e1
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GenotypeQuality
all individuals: 1577
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514142087093453e-5
allele num: 66044
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.920634920634921e-5
allele num: 10080
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European (Non-Finnish)
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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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East Asian
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Other
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8636
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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Latino
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Other
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VQSLOD
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DP
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MQ
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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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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Latino
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allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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African
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South Asian
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allele frequency: 0.0e0
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 9.071940488070398e-5
allele num: 66138
num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: 3.36e-1

QD
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.904e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

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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allele frequency: 1.512035805007863e-5
allele num: 66136
num of homozygotes: 0

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

African
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European (Non-Finnish)
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allele num: 66142
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East Asian
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Other
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European (Finnish)
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Latino
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FS
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DP
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MQRankSum
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QD
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66160
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African
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European (Finnish)
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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QD
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

East Asian
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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QD
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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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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43679
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1508
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
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: 11554
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.409e1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

DP
type: SiteQuality
SIO_000300: 3.825883e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e0

FS
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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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: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.058393056941546e-4
allele num: 66138
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.486e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

DP
type: SiteQuality
SIO_000300: 3.823145e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 9.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

GenotypeQuality
all individuals: 5197
bin: 6.25e1
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
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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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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
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: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
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: 11554
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

QD
type: SiteQuality
SIO_000300: 1.486e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 9.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 3.823145e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 636
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variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.814718e6

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.35e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

GenotypeQuality
all individuals: 44080
bin: 9.75e1
variant carriers: 1475

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 780
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 1704
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variant carriers: 1

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 21
allele frequency: 2.081681205392546e-3
allele num: 10088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 2.875302663438257e-3
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 378
allele frequency: 5.721897611334807e-3
allele num: 66062
num of homozygotes: 0

East Asian
type: Population
allele count: 195
allele frequency: 2.264808362369338e-2
allele num: 8610
num of homozygotes: 1

Latino
type: Population
allele count: 41
allele frequency: 3.551013337952537e-3
allele num: 11546
num of homozygotes: 1

South Asian
type: Population
allele count: 880
allele frequency: 5.372405372405373e-2
allele num: 16380
num of homozygotes: 52

Other
type: Population
allele count: 14
allele frequency: 1.55902004454343e-2
allele num: 898
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.803119e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

QD
type: SiteQuality
SIO_000300: 1.539e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

GenotypeDepth
all individuals: 1000
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1165
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3514
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2083
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variant carriers: 0

GenotypeDepth
all individuals: 296
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GenotypeDepth
all individuals: 5348
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variant carriers: 0

GenotypeDepth
all individuals: 939
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GenotypeDepth
all individuals: 669
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 86
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variant carriers: 0

GenotypeDepth
all individuals: 129
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GenotypeDepth
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GenotypeQuality
all individuals: 1062
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3656
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15929
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variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.122691572914456e-4
allele num: 9422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
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: 8552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.099e1

MQ
type: SiteQuality
SIO_000300: 5.838e1

FS
type: SiteQuality
SIO_000300: 6.947e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -8.304e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 2.226551e6

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9080
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 327
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GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 12036
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variant carriers: 0

GenotypeDepth
all individuals: 383
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variant carriers: 0

GenotypeDepth
all individuals: 10604
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variant carriers: 0

GenotypeDepth
all individuals: 247
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GenotypeDepth
all individuals: 86
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variant carriers: 0

GenotypeDepth
all individuals: 669
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variant carriers: 0

GenotypeDepth
all individuals: 129
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variant carriers: 0

GenotypeDepth
all individuals: 2083
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variant carriers: 0

GenotypeDepth
all individuals: 5349
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 262
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6551
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
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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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bin: 4.75e1
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GenotypeQuality
all individuals: 15883
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532144389287247e-5
allele num: 65268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.226848e6

FS
type: SiteQuality
SIO_000300: 1.5152e1

QD
type: SiteQuality
SIO_000300: 1.039e1

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.218e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

GenotypeDepth
all individuals: 10625
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12053
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 930
bin: 7.5e0
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GenotypeDepth
all individuals: 939
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variant carriers: 0

GenotypeDepth
all individuals: 356
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variant carriers: 0

GenotypeDepth
all individuals: 9081
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variant carriers: 0

GenotypeDepth
all individuals: 129
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variant carriers: 0

GenotypeDepth
all individuals: 248
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variant carriers: 1

GenotypeDepth
all individuals: 1164
bin: 6.25e1
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 383
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GenotypeDepth
all individuals: 4994
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variant carriers: 0

GenotypeDepth
all individuals: 7288
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
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GenotypeQuality
all individuals: 4619
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GenotypeQuality
all individuals: 94
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GenotypeQuality
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GenotypeQuality
all individuals: 324
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 143
bin: 4.75e1
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GenotypeQuality
all individuals: 2773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 3657
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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Other
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MQ
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SIO_000300: 5.566e1

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -1.47e-1

ReadPosRankSum
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DP
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SIO_000300: 2.231179e6

MQRankSum
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MQ
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SIO_000300: 5.417e1

VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 1.08e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 2.73e-2

GenotypeDepth
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variant carriers: 0

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

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

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

African
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allele count: 1
allele frequency: 1.083423618634886e-4
allele num: 9230
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

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

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

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

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

MQRankSum
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SIO_000300: -2.5e-2

ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.854e1

BaseQRankSum
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SIO_000300: -4.621e0

FS
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SIO_000300: 6.38e-1

ReadPosRankSum
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SIO_000300: -1.314e0

DP
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SIO_000300: 2.218103e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544592382070372e-5
allele num: 64742
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9206
num of homozygotes: 0

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

East Asian
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allele count: 3
allele frequency: 3.513703443429375e-4
allele num: 8538
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

VQSLOD
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SIO_000300: -6.086e-1

FS
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SIO_000300: 0.0e0

MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 2.3e-3

ClippingRankSum
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SIO_000300: -3.61e-1

QD
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SIO_000300: 1.121e1

MQ
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SIO_000300: 5.881e1

BaseQRankSum
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SIO_000300: -3.625e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 47

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

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
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African
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allele count: 44
allele frequency: 4.77845351867941e-3
allele num: 9208
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.545547278291243e-5
allele num: 64702
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.3e-3

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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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