http://identifiers.org/exac.variant/19-44733891-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733891
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733891
    reference: chr 19
allele count: 1
allele frequency: 8.403785064793184e-6
allele num: 118994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.40C>A
  hgvsp: ENSP00000375823.2:p.Leu14Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.40C>A
  hgvsp: ENSP00000467577.1:p.Leu14Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.193C>A
  hgvsp: ENSP00000321049.6:p.Leu65Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.152C>A
  hgvsp: ENSP00000467496.1:p.Ser51Tyr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1166C>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-775G>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1166C>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464800
  ensembl transcript: ENST00000586048
  gene symbol: ZNF227
  hgvsc: ENST00000586048.1:c.193C>A
  hgvsp: ENSP00000464800.1:p.Leu65Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1105C>A
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu65Ile
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

19-44733920-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733920
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733920
    reference: chr 19
allele count: 3
allele frequency: 2.492936679408343e-5
allele num: 120340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1134A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.69A>G
  hgvsp: ENST00000391961.2:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.69A>G
  hgvsp: ENST00000589005.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1195A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.181A>G
  hgvsp: ENSP00000467496.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.222A>G
  hgvsp: ENST00000313040.7:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1195A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464800
  ensembl transcript: ENST00000586048
  gene symbol: ZNF227
  hgvsc: ENST00000586048.1:c.222A>G
  hgvsp: ENST00000586048.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-804T>C
  variant of: http://identifiers.org/hgnc/12866
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16006
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35540
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46463
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile61Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-44733928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733928
    reference: chr 19
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-812G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1203C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.77C>T
  hgvsp: ENSP00000467577.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.189C>T
  hgvsp: ENST00000586228.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1203C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464800
  ensembl transcript: ENST00000586048
  gene symbol: ZNF227
  hgvsc: ENST00000586048.1:c.230C>T
  hgvsp: ENSP00000464800.1:p.Ala77Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.77C>T
  hgvsp: ENSP00000375823.2:p.Ala26Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.230C>T
  hgvsp: ENSP00000321049.6:p.Ala77Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1142C>T
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala77Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

19-44733939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733939
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733939
    reference: chr 19
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1214C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.241C>T
  hgvsp: ENSP00000321049.6:p.Leu81Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-823G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.88C>T
  hgvsp: ENSP00000467577.1:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.200C>T
  hgvsp: ENSP00000467496.1:p.Ala67Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1153C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464800
  ensembl transcript: ENST00000586048
  gene symbol: ZNF227
  hgvsc: ENST00000586048.1:c.241C>T
  hgvsp: ENSP00000464800.1:p.Leu81Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.88C>T
  hgvsp: ENSP00000375823.2:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1214C>T
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu81Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-44733941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733941
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733941
    reference: chr 19
allele count: 1
allele frequency: 8.320021299254527e-6
allele num: 120192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-825A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1155T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.202T>C
  hgvsp: ENST00000586228.1:c.202T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.90T>C
  hgvsp: ENST00000391961.2:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.90T>C
  hgvsp: ENST00000589005.1:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1216T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.243T>C
  hgvsp: ENST00000313040.7:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464800
  ensembl transcript: ENST00000586048
  gene symbol: ZNF227
  hgvsc: ENST00000586048.1:c.243T>C
  hgvsp: ENST00000586048.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1216T>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu81Leu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

19-44733949-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733949
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733949
    reference: chr 19
allele count: 3
allele frequency: 2.503797426096246e-5
allele num: 119818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1224T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.98T>C
  hgvsp: ENSP00000467577.1:p.Met33Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-833A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1163T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1224T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.251T>C
  hgvsp: ENSP00000321049.6:p.Met84Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.98T>C
  hgvsp: ENSP00000375823.2:p.Met33Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.210T>C
  hgvsp: ENST00000586228.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met84Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

19-44733977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733977
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733977
    reference: chr 19
allele count: 1
allele frequency: 8.56956775100264e-6
allele num: 116692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+8T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1252T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-861A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+8T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+8T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+8T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1252T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1191T>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 9.25e1
  variant carriers: 0
hgvs: c.271+8T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

19-44733982-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733982
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733983
    reference: chr 19
allele count: 1
allele frequency: 8.621432882145012e-6
allele num: 115990
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+14dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1258dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1258dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1197dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+14dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-867dupA
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+14dupT
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+14dupT
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5911
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-44733987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733987
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733987
    reference: chr 19
allele count: 2
allele frequency: 1.73235166738848e-5
allele num: 115450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+18A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+18A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1201A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1262A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-871T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+18A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+18A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1262A>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-44733988-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733988
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733988
    reference: chr 19
allele count: 9
allele frequency: 7.807755703999306e-5
allele num: 115270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1202A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-872T>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1263A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+19A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+19A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1263A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+19A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+19A>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4237
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-44733992-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733992
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733992
    reference: chr 19
allele count: 111
allele frequency: 9.67539486070918e-4
allele num: 114724
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-876A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+23T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1206T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+23T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+23T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1267T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+23T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1267T>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10959
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-44733999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44733999
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44733999
    reference: chr 19
allele count: 16
allele frequency: 1.411806229594988e-4
allele num: 113330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1213G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+30G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1274G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+30G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+30G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+30G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1274G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-883C>T
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9932
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13404
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15199
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

19-44734008-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44734008
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44734008
    reference: chr 19
allele count: 1
allele frequency: 8.924427944168779e-6
allele num: 112052
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+39G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1283G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1283G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+39G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-892C>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+39G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1222G>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+39G>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8830
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

19-44734012-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44734012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44734012
    reference: chr 19
allele count: 1
allele frequency: 9.046335329557996e-6
allele num: 110542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1287C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+43C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-896G>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1287C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1226C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+43C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+43C>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+43C>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3364
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4866
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-44734012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44734012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44734012
    reference: chr 19
allele count: 1
allele frequency: 9.046335329557996e-6
allele num: 110542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.118+43C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.95+1226C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.271+43C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.187+1287C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.118+43C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.34+1287C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*108-896G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.230+43C>T
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16307
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

19-44738809-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738809
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738809
    reference: chr 19
allele count: 12
allele frequency: 1.446201311222522e-4
allele num: 82976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+99A>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-46T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-46T>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18507
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13528
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5914
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-44738813-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738813
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738813
    reference: chr 19
allele count: 1
allele frequency: 1.207962891379977e-5
allele num: 82784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+95G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-42C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-42C>T
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9840
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4573
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7823
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-44738844-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738844
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738844
    reference: chr 19
allele count: 3
allele frequency: 3.001260529422357e-5
allele num: 99958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-11T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+64A>C
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-44738846-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738846
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738846
    reference: chr 19
allele count: 2
allele frequency: 1.971880977264212e-5
allele num: 101426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+62A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-9T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-9T>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-44738849-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738849
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738849
    reference: chr 19
allele count: 2
allele frequency: 1.931546009425944e-5
allele num: 103544
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-6T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+59A>C
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37436
  bin: 6.25e1
  variant carriers: 0
hgvs: c.272-6T>G
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: T
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

19-44738851-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738851
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738851
    reference: chr 19
allele count: 2
allele frequency: 1.905633051299642e-5
allele num: 104952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.35-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.96-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.272-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.188-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+57T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.119-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.119-4A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.231-4A>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39018
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7305
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 9.75e1
  variant carriers: 2
hgvs: c.272-4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-44738856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738856
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738856
    reference: chr 19
allele count: 1
allele frequency: 9.278675747397332e-6
allele num: 107774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+52G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.273C>T
  hgvsp: ENST00000313040.7:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.232C>T
  hgvsp: ENSP00000467496.1:p.Gln78Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.120C>T
  hgvsp: ENST00000589005.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.189C>T
  hgvsp: ENST00000588394.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.36C>T
  hgvsp: ENST00000588219.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.120C>T
  hgvsp: ENST00000391961.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.97C>T
  hgvsp: ENSP00000465071.1:p.Gln33Ter
  variant of: http://identifiers.org/hgnc/13020
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39985
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln33Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-44738859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738859
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738859
    reference: chr 19
allele count: 1
allele frequency: 9.150805270863836e-6
allele num: 109280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+49G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.100C>T
  hgvsp: ENSP00000465071.1:p.Gln34Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.276C>T
  hgvsp: ENST00000313040.7:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.123C>T
  hgvsp: ENST00000589005.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.192C>T
  hgvsp: ENST00000588394.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.235C>T
  hgvsp: ENSP00000467496.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.39C>T
  hgvsp: ENST00000588219.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.123C>T
  hgvsp: ENST00000391961.2:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln34Ter
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

19-44738864-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738864
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738864
    reference: chr 19
allele count: 7
allele frequency: 6.280956140980547e-5
allele num: 111448
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.281A>T
  hgvsp: ENSP00000321049.6:p.His94Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.240A>T
  hgvsp: ENST00000586228.1:c.240A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.197A>T
  hgvsp: ENSP00000466197.1:p.His66Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.128A>T
  hgvsp: ENSP00000375823.2:p.His43Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.105A>T
  hgvsp: ENST00000589707.1:c.105A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.44A>T
  hgvsp: ENSP00000464866.1:p.His15Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.128A>T
  hgvsp: ENSP00000467577.1:p.His43Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+44T>A
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His94Leu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

19-44738870-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738870
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738870
    reference: chr 19
allele count: 1
allele frequency: 8.862105636299185e-6
allele num: 112840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+38T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.287A>G
  hgvsp: ENSP00000321049.6:p.Asn96Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.246A>G
  hgvsp: ENST00000586228.1:c.246A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.50A>G
  hgvsp: ENSP00000464866.1:p.Asn17Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.134A>G
  hgvsp: ENSP00000375823.2:p.Asn45Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.134A>G
  hgvsp: ENSP00000467577.1:p.Asn45Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.203A>G
  hgvsp: ENSP00000466197.1:p.Asn68Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.111A>G
  hgvsp: ENST00000589707.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41480
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4098
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn96Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-44738876-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738876
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738876
    reference: chr 19
allele count: 1
allele frequency: 8.758868354208636e-6
allele num: 114170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.140T>C
  hgvsp: ENSP00000467577.1:p.Met47Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+32A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.56T>C
  hgvsp: ENSP00000464866.1:p.Met19Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*3T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.209T>C
  hgvsp: ENSP00000466197.1:p.Met70Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*3T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.293T>C
  hgvsp: ENSP00000321049.6:p.Met98Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.140T>C
  hgvsp: ENSP00000375823.2:p.Met47Thr
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met98Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-44738879-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738879
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738879
    reference: chr 19
allele count: 5
allele frequency: 4.355476576246973e-5
allele num: 114798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*6A>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.296A>T
  hgvsp: ENSP00000321049.6:p.Glu99Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+29T>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.143A>T
  hgvsp: ENSP00000375823.2:p.Glu48Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.143A>T
  hgvsp: ENSP00000467577.1:p.Glu48Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.59A>T
  hgvsp: ENSP00000464866.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.212A>T
  hgvsp: ENSP00000466197.1:p.Glu71Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*6A>T
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu99Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

19-44738882-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738882
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738882
    reference: chr 19
allele count: 1
allele frequency: 8.67362869930264e-6
allele num: 115292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.62C>T
  hgvsp: ENSP00000464866.1:p.Thr21Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.146C>T
  hgvsp: ENSP00000375823.2:p.Thr49Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.146C>T
  hgvsp: ENSP00000467577.1:p.Thr49Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.215C>T
  hgvsp: ENSP00000466197.1:p.Thr72Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.299C>T
  hgvsp: ENSP00000321049.6:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+26G>A
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr100Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-44738892-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738892
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738892
    reference: chr 19
allele count: 1
allele frequency: 8.512521919743944e-6
allele num: 117474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.72A>C
  hgvsp: ENSP00000464866.1:p.Lys24Asn
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.225A>C
  hgvsp: ENSP00000466197.1:p.Lys75Asn
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.309A>C
  hgvsp: ENSP00000321049.6:p.Lys103Asn
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+16T>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.156A>C
  hgvsp: ENSP00000375823.2:p.Lys52Asn
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*19A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*19A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.156A>C
  hgvsp: ENSP00000467577.1:p.Lys52Asn
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5791
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys103Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-44738894-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738894
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738894
    reference: chr 19
allele count: 1
allele frequency: 8.488964346349745e-6
allele num: 117800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.158T>G
  hgvsp: ENSP00000375823.2:p.Phe53Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.158T>G
  hgvsp: ENSP00000467577.1:p.Phe53Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.311T>G
  hgvsp: ENSP00000321049.6:p.Phe104Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*21T>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.74T>G
  hgvsp: ENSP00000464866.1:p.Phe25Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.227T>G
  hgvsp: ENSP00000466197.1:p.Phe76Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+14A>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*21T>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43837
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe104Cys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-44738898-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738898
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738898
    reference: chr 19
allele count: 1
allele frequency: 8.449085808915476e-6
allele num: 118356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.162A>G
  hgvsp: ENST00000589005.1:c.162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.315A>G
  hgvsp: ENST00000313040.7:c.315A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.78A>G
  hgvsp: ENST00000588219.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.162A>G
  hgvsp: ENST00000391961.2:c.162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*25A>G
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*107+10T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.231A>G
  hgvsp: ENST00000588394.1:c.231A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*25A>G
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala105Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-44738919-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738919
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738919
    reference: chr 19
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.99A>C
  hgvsp: ENSP00000464866.1:p.Gln33His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.183A>C
  hgvsp: ENSP00000467577.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.336A>C
  hgvsp: ENSP00000321049.6:p.Gln112His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*96T>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*46A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.252A>C
  hgvsp: ENSP00000466197.1:p.Gln84His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*46A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.183A>C
  hgvsp: ENSP00000375823.2:p.Gln61His
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln112His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

19-44738922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738922
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738922
    reference: chr 19
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.102G>A
  hgvsp: ENST00000588219.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.255G>A
  hgvsp: ENST00000588394.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.186G>A
  hgvsp: ENST00000391961.2:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*49G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.186G>A
  hgvsp: ENST00000589005.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.339G>A
  hgvsp: ENST00000313040.7:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*49G>A
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu113Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-44738927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738927
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738927
    reference: chr 19
allele count: 18
allele frequency: 1.493255462826235e-4
allele num: 120542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*88G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.191C>T
  hgvsp: ENSP00000467577.1:p.Ser64Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.344C>T
  hgvsp: ENSP00000321049.6:p.Ser115Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.107C>T
  hgvsp: ENSP00000464866.1:p.Ser36Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.191C>T
  hgvsp: ENSP00000375823.2:p.Ser64Phe
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.260C>T
  hgvsp: ENSP00000466197.1:p.Ser87Phe
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser115Phe
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS

19-44738929-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738929
    reference: chr 19
allele count: 7
allele frequency: 5.805370797326212e-5
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*86A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*56T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.109T>C
  hgvsp: ENSP00000464866.1:p.Cys37Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.262T>C
  hgvsp: ENSP00000466197.1:p.Cys88Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.193T>C
  hgvsp: ENSP00000467577.1:p.Cys65Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.193T>C
  hgvsp: ENSP00000375823.2:p.Cys65Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*56T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.346T>C
  hgvsp: ENSP00000321049.6:p.Cys116Arg
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys116Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

19-44738934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738934
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738934
    reference: chr 19
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.267G>A
  hgvsp: ENSP00000466197.1:p.Trp89Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.351G>A
  hgvsp: ENSP00000321049.6:p.Trp117Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.198G>A
  hgvsp: ENSP00000375823.2:p.Trp66Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.198G>A
  hgvsp: ENSP00000467577.1:p.Trp66Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.114G>A
  hgvsp: ENSP00000464866.1:p.Trp38Ter
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*61G>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*61G>A
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Trp117Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/19-44738940-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738940
    reference: chr 19
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.204C>A
  hgvsp: ENST00000391961.2:c.204C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.273C>A
  hgvsp: ENST00000588394.1:c.273C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.204C>A
  hgvsp: ENST00000589005.1:c.204C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.357C>A
  hgvsp: ENST00000313040.7:c.357C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.120C>A
  hgvsp: ENST00000588219.1:c.120C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*67C>A
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*75G>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*67C>A
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile119Ile
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

19-44738962-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738962
    reference: chr 19
allele count: 3
allele frequency: 2.482046530098951e-5
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.226T>C
  hgvsp: ENST00000589005.1:c.226T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.142T>C
  hgvsp: ENST00000588219.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.295T>C
  hgvsp: ENST00000588394.1:c.295T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.379T>C
  hgvsp: ENST00000313040.7:c.379T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.226T>C
  hgvsp: ENST00000391961.2:c.226T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*89T>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*53A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*89T>C
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6092
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu127Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-44738978-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738978
    reference: chr 19
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*37T>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.242A>C
  hgvsp: ENSP00000467577.1:p.Gln81Pro
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*105A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*105A>C
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.395A>C
  hgvsp: ENSP00000321049.6:p.Gln132Pro
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.242A>C
  hgvsp: ENSP00000375823.2:p.Gln81Pro
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.158A>C
  hgvsp: ENSP00000464866.1:p.Gln53Pro
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.311A>C
  hgvsp: ENSP00000466197.1:p.Gln104Pro
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln132Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

19-44738979-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738979
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738979
    reference: chr 19
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000465071
  ensembl transcript: ENST00000589707
  gene symbol: ZNF227
  hgvsc: ENST00000589707.1:c.*106G>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.396G>T
  hgvsp: ENSP00000321049.6:p.Gln132His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.159G>T
  hgvsp: ENSP00000464866.1:p.Gln53His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.312G>T
  hgvsp: ENSP00000466197.1:p.Gln104His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467496
  ensembl transcript: ENST00000586228
  gene symbol: ZNF227
  hgvsc: ENST00000586228.1:c.*106G>T
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.243G>T
  hgvsp: ENSP00000467577.1:p.Gln81His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*36C>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.243G>T
  hgvsp: ENSP00000375823.2:p.Gln81His
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln132His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

19-44738995-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44738995
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44738995
    reference: chr 19
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.175T>A
  hgvsp: ENSP00000464866.1:p.Leu59Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.328T>A
  hgvsp: ENSP00000466197.1:p.Leu110Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.412T>A
  hgvsp: ENSP00000321049.6:p.Leu138Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.259T>A
  hgvsp: ENSP00000375823.2:p.Leu87Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.259T>A
  hgvsp: ENSP00000467577.1:p.Leu87Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*20A>T
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6093
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu138Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-44739003-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739003
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739003
    reference: chr 19
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.336A>C
  hgvsp: ENSP00000466197.1:p.Gln112His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.183A>C
  hgvsp: ENSP00000464866.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.420A>C
  hgvsp: ENSP00000321049.6:p.Gln140His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.267A>C
  hgvsp: ENSP00000467577.1:p.Gln89His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.267A>C
  hgvsp: ENSP00000375823.2:p.Gln89His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*12T>G
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9836
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln140His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

19-44739006-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739006
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739006
    reference: chr 19
allele count: 2
allele frequency: 1.656808655168415e-5
allele num: 120714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.270T>G
  hgvsp: ENST00000589005.1:c.270T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.339T>G
  hgvsp: ENST00000588394.1:c.339T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*9A>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.423T>G
  hgvsp: ENST00000313040.7:c.423T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.186T>G
  hgvsp: ENST00000588219.1:c.186T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.270T>G
  hgvsp: ENST00000391961.2:c.270T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45189
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly141Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-44739011-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739011
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739011
    reference: chr 19
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.344C>G
  hgvsp: ENSP00000466197.1:p.Ser115Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.275C>G
  hgvsp: ENSP00000467577.1:p.Ser92Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.191C>G
  hgvsp: ENSP00000464866.1:p.Ser64Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.428C>G
  hgvsp: ENSP00000321049.6:p.Ser143Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.275C>G
  hgvsp: ENSP00000375823.2:p.Ser92Cys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.*4G>C
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6079
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser143Cys
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

19-44739016-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739016
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739016
    reference: chr 19
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.349C>G
  hgvsp: ENSP00000466197.1:p.Gln117Glu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.433C>G
  hgvsp: ENSP00000321049.6:p.Gln145Glu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.196C>G
  hgvsp: ENSP00000464866.1:p.Gln66Glu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.280C>G
  hgvsp: ENSP00000467577.1:p.Gln94Glu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.245G>C
  hgvsp: ENSP00000465641.1:p.Ter82SerextTer13
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.280C>G
  hgvsp: ENSP00000375823.2:p.Gln94Glu
  variant of: http://identifiers.org/hgnc/13020
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45031
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6075
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ter82SerextTer13
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

19-44739029-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739029
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739029
    reference: chr 19
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.209A>T
  hgvsp: ENSP00000464866.1:p.Asn70Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.293A>T
  hgvsp: ENSP00000467577.1:p.Asn98Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.362A>T
  hgvsp: ENSP00000466197.1:p.Asn121Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.446A>T
  hgvsp: ENSP00000321049.6:p.Asn149Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-7T>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.293A>T
  hgvsp: ENSP00000375823.2:p.Asn98Ile
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn149Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-44739031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739031
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739031
    reference: chr 19
allele count: 613
allele frequency: 5.085701959613055e-3
allele num: 120534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.295G>A
  hgvsp: ENSP00000467577.1:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.364G>A
  hgvsp: ENSP00000466197.1:p.Glu122Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-9C>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.211G>A
  hgvsp: ENSP00000464866.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.295G>A
  hgvsp: ENSP00000375823.2:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.448G>A
  hgvsp: ENSP00000321049.6:p.Glu150Lys
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43545
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44426
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu150Lys
num of homozygotes: 14
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-44739033-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739033
    reference: chr 19
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.297G>A
  hgvsp: ENST00000589005.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.297G>A
  hgvsp: ENST00000391961.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.366G>A
  hgvsp: ENST00000588394.1:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.450G>A
  hgvsp: ENST00000313040.7:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.213G>A
  hgvsp: ENST00000588219.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-11C>T
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu150Glu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

19-44739036-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739036
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739036
    reference: chr 19
allele count: 5
allele frequency: 4.15020419004615e-5
allele num: 120476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.300C>T
  hgvsp: ENST00000391961.2:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.300C>T
  hgvsp: ENST00000589005.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.216C>T
  hgvsp: ENST00000588219.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-14G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.369C>T
  hgvsp: ENST00000588394.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.453C>T
  hgvsp: ENST00000313040.7:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn151Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-44739040-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739040
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739040
    reference: chr 19
allele count: 1
allele frequency: 8.302062232258493e-6
allele num: 120452
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.457A>G
  hgvsp: ENSP00000321049.6:p.Ile153Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.304A>G
  hgvsp: ENSP00000467577.1:p.Ile102Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-18T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.304A>G
  hgvsp: ENSP00000375823.2:p.Ile102Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.373A>G
  hgvsp: ENSP00000466197.1:p.Ile125Val
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.220A>G
  hgvsp: ENSP00000464866.1:p.Ile74Val
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44347
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile153Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

19-44739041-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739041
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739041
    reference: chr 19
allele count: 3
allele frequency: 2.491032283778398e-5
allele num: 120432
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.305T>C
  hgvsp: ENSP00000375823.2:p.Ile102Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.305T>C
  hgvsp: ENSP00000467577.1:p.Ile102Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.458T>C
  hgvsp: ENSP00000321049.6:p.Ile153Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-19A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.221T>C
  hgvsp: ENSP00000464866.1:p.Ile74Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.374T>C
  hgvsp: ENSP00000466197.1:p.Ile125Thr
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile153Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-44739044-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739044
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739044
    reference: chr 19
allele count: 3
allele frequency: 2.491073652744333e-5
allele num: 120430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-22A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.224T>C
  hgvsp: ENSP00000464866.1:p.Met75Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.308T>C
  hgvsp: ENSP00000467577.1:p.Met103Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.377T>C
  hgvsp: ENSP00000466197.1:p.Met126Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.461T>C
  hgvsp: ENSP00000321049.6:p.Met154Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.308T>C
  hgvsp: ENSP00000375823.2:p.Met103Thr
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met154Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-44739048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739048
    reference: chr 19
allele count: 2
allele frequency: 1.661212352775055e-5
allele num: 120394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.312C>T
  hgvsp: ENST00000589005.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.381C>T
  hgvsp: ENST00000588394.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.465C>T
  hgvsp: ENST00000313040.7:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.312C>T
  hgvsp: ENST00000391961.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.228C>T
  hgvsp: ENST00000588219.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-26G>A
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44194
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn155Asn
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-44739053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739053
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739053
    reference: chr 19
allele count: 2
allele frequency: 1.661377946869133e-5
allele num: 120382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-31T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.317A>G
  hgvsp: ENSP00000375823.2:p.Lys106Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.233A>G
  hgvsp: ENSP00000464866.1:p.Lys78Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.317A>G
  hgvsp: ENSP00000467577.1:p.Lys106Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.470A>G
  hgvsp: ENSP00000321049.6:p.Lys157Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.386A>G
  hgvsp: ENSP00000466197.1:p.Lys129Arg
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys157Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

19-44739056-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739056
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739056
    reference: chr 19
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.473G>C
  hgvsp: ENSP00000321049.6:p.Gly158Ala
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.320G>C
  hgvsp: ENSP00000467577.1:p.Gly107Ala
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.236G>C
  hgvsp: ENSP00000464866.1:p.Gly79Ala
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.320G>C
  hgvsp: ENSP00000375823.2:p.Gly107Ala
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-34C>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.389G>C
  hgvsp: ENSP00000466197.1:p.Gly130Ala
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6023
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly158Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

19-44739074-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739074
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739074
    reference: chr 19
allele count: 1
allele frequency: 8.316838270762986e-6
allele num: 120238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.254T>C
  hgvsp: ENSP00000464866.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.338T>C
  hgvsp: ENSP00000375823.2:p.Ile113Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.407T>C
  hgvsp: ENSP00000466197.1:p.Ile136Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.491T>C
  hgvsp: ENSP00000321049.6:p.Ile164Thr
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-52A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.338T>C
  hgvsp: ENSP00000467577.1:p.Ile113Thr
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile164Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-44739076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739076
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739076
    reference: chr 19
allele count: 1
allele frequency: 8.31849867735871e-6
allele num: 120214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-54C>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.493G>A
  hgvsp: ENSP00000321049.6:p.Glu165Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.409G>A
  hgvsp: ENSP00000466197.1:p.Glu137Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.340G>A
  hgvsp: ENSP00000375823.2:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.256G>A
  hgvsp: ENSP00000464866.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.340G>A
  hgvsp: ENSP00000467577.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6032
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu165Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

19-44739079-A-AATC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739079
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739082
    reference: chr 19
allele count: 5
allele frequency: 4.158765013141698e-5
allele num: 120228
alternate allele: AATC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.345_347dupTCA
  hgvsp: ENSP00000375823.2:p.Asn115_Gln116insHis
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.498_500dupTCA
  hgvsp: ENSP00000321049.6:p.Asn166_Gln167insHis
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.414_416dupTCA
  hgvsp: ENSP00000466197.1:p.Asn138_Gln139insHis
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.261_263dupTCA
  hgvsp: ENSP00000464866.1:p.Asn87_Gln88insHis
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-60_239-58dupGAT
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.345_347dupTCA
  hgvsp: ENSP00000467577.1:p.Asn115_Gln116insHis
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn166_Gln167insHis
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-44739090-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739089
    reference: chr 19
allele count: 1
allele frequency: 8.319882856049386e-6
allele num: 120194
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.509delC
  hgvsp: ENSP00000321049.6:p.Pro170HisfsTer14
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.356delC
  hgvsp: ENSP00000375823.2:p.Pro119HisfsTer14
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.356delC
  hgvsp: ENSP00000467577.1:p.Pro119HisfsTer14
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.425delC
  hgvsp: ENSP00000466197.1:p.Pro142HisfsTer14
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-69delG
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.272delC
  hgvsp: ENSP00000464866.1:p.Pro91HisfsTer?
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro170HisfsTer14
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: TC
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-44739091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739091
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739091
    reference: chr 19
allele count: 1
allele frequency: 8.322929671244279e-6
allele num: 120150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.355C>T
  hgvsp: ENSP00000467577.1:p.Pro119Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-69G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.424C>T
  hgvsp: ENSP00000466197.1:p.Pro142Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.355C>T
  hgvsp: ENSP00000375823.2:p.Pro119Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.271C>T
  hgvsp: ENSP00000464866.1:p.Pro91Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.508C>T
  hgvsp: ENSP00000321049.6:p.Pro170Ser
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro170Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-44739094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739094
    reference: chr 19
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.274T>C
  hgvsp: ENSP00000464866.1:p.Phe92Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.511T>C
  hgvsp: ENSP00000321049.6:p.Phe171Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.358T>C
  hgvsp: ENSP00000375823.2:p.Phe120Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.358T>C
  hgvsp: ENSP00000467577.1:p.Phe120Leu
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-72A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.427T>C
  hgvsp: ENSP00000466197.1:p.Phe143Leu
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe171Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-44739095-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739095
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739095
    reference: chr 19
allele count: 5
allele frequency: 4.160979994008189e-5
allele num: 120164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.359T>C
  hgvsp: ENSP00000375823.2:p.Phe120Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-73A>G
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.428T>C
  hgvsp: ENSP00000466197.1:p.Phe143Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.512T>C
  hgvsp: ENSP00000321049.6:p.Phe171Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.275T>C
  hgvsp: ENSP00000464866.1:p.Phe92Ser
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.359T>C
  hgvsp: ENSP00000467577.1:p.Phe120Ser
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe171Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

19-44739105-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739105
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739105
    reference: chr 19
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.438C>G
  hgvsp: ENST00000588394.1:c.438C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.369C>G
  hgvsp: ENST00000589005.1:c.369C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.285C>G
  hgvsp: ENST00000588219.1:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.369C>G
  hgvsp: ENST00000391961.2:c.369C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.522C>G
  hgvsp: ENST00000313040.7:c.522C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-83G>C
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr174Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

19-44739108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739108
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739108
    reference: chr 19
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.525G>A
  hgvsp: ENST00000313040.7:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.372G>A
  hgvsp: ENST00000391961.2:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.372G>A
  hgvsp: ENST00000589005.1:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000464866
  ensembl transcript: ENST00000588219
  gene symbol: ZNF227
  hgvsc: ENST00000588219.1:c.288G>A
  hgvsp: ENST00000588219.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.441G>A
  hgvsp: ENST00000588394.1:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-86C>T
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln175Gln
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

19-44739110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739110
    reference: chr 19
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.443A>G
  hgvsp: ENSP00000466197.1:p.His148Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.374A>G
  hgvsp: ENSP00000467577.1:p.His125Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.374A>G
  hgvsp: ENSP00000375823.2:p.His125Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-88T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.527A>G
  hgvsp: ENSP00000321049.6:p.His176Arg
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6180
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His176Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-44739117-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739117
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739117
    reference: chr 19
allele count: 5
allele frequency: 4.160979994008189e-5
allele num: 120164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-95G>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.381C>G
  hgvsp: ENSP00000375823.2:p.Cys127Trp
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.381C>G
  hgvsp: ENSP00000467577.1:p.Cys127Trp
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.534C>G
  hgvsp: ENSP00000321049.6:p.Cys178Trp
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.450C>G
  hgvsp: ENSP00000466197.1:p.Cys150Trp
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43531
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys178Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-44739117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739117
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739117
    reference: chr 19
allele count: 29
allele frequency: 2.413368396524749e-4
allele num: 120164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.381C>T
  hgvsp: ENST00000589005.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.450C>T
  hgvsp: ENST00000588394.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-95G>A
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.534C>T
  hgvsp: ENST00000313040.7:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.381C>T
  hgvsp: ENST00000391961.2:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42309
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 9.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys178Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-44739118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739118
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739118
    reference: chr 19
allele count: 3
allele frequency: 2.496837339370131e-5
allele num: 120152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-96C>T
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.382G>A
  hgvsp: ENSP00000467577.1:p.Gly128Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.451G>A
  hgvsp: ENSP00000466197.1:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.382G>A
  hgvsp: ENSP00000375823.2:p.Gly128Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.535G>A
  hgvsp: ENSP00000321049.6:p.Gly179Arg
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43530
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly179Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

19-44739125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739125
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739125
    reference: chr 19
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.458C>T
  hgvsp: ENSP00000466197.1:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.389C>T
  hgvsp: ENSP00000375823.2:p.Thr130Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.389C>T
  hgvsp: ENSP00000467577.1:p.Thr130Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.542C>T
  hgvsp: ENSP00000321049.6:p.Thr181Ile
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-103G>A
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6238
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr181Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

19-44739126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739126
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739126
    reference: chr 19
allele count: 3
allele frequency: 2.49613099695472e-5
allele num: 120186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-104T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.390A>G
  hgvsp: ENST00000391961.2:c.390A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.459A>G
  hgvsp: ENST00000588394.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.390A>G
  hgvsp: ENST00000589005.1:c.390A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.543A>G
  hgvsp: ENST00000313040.7:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr181Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-44739127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739127
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739127
    reference: chr 19
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.460T>C
  hgvsp: ENSP00000466197.1:p.Tyr154His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.391T>C
  hgvsp: ENSP00000375823.2:p.Tyr131His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.544T>C
  hgvsp: ENSP00000321049.6:p.Tyr182His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.391T>C
  hgvsp: ENSP00000467577.1:p.Tyr131His
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-105A>G
  variant of: http://identifiers.org/hgnc/12866
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6250
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr182His
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-44739164-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44739164
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 44739164
    reference: chr 19
allele count: 1
allele frequency: 8.314487162431821e-6
allele num: 120272
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000321049
  ensembl transcript: ENST00000313040
  gene symbol: ZNF227
  hgvsc: ENST00000313040.7:c.581A>G
  hgvsp: ENSP00000321049.6:p.Gln194Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000467577
  ensembl transcript: ENST00000589005
  gene symbol: ZNF227
  hgvsc: ENST00000589005.1:c.428A>G
  hgvsp: ENSP00000467577.1:p.Gln143Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159917
  ensembl protein: ENSP00000465641
  ensembl transcript: ENST00000592844
  gene symbol: ZNF235
  hgvsc: ENST00000592844.1:c.239-142T>C
  variant of: http://identifiers.org/hgnc/12866
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000375823
  ensembl transcript: ENST00000391961
  gene symbol: ZNF227
  hgvsc: ENST00000391961.2:c.428A>G
  hgvsp: ENSP00000375823.2:p.Gln143Arg
  variant of: http://identifiers.org/hgnc/13020
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000131115
  ensembl protein: ENSP00000466197
  ensembl transcript: ENST00000588394
  gene symbol: ZNF227
  hgvsc: ENST00000588394.1:c.497A>G
  hgvsp: ENSP00000466197.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/13020
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln194Arg
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5006
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520403819254394e-5
allele num: 65772
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.131e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 1.681376e6

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5091
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509707418702255e-5
allele num: 66238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.216585851050602e-5
allele num: 16086
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.701371e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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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: 394
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
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: 16100
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.702222e6

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 4.168e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 749
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 146
bin: 2.75e1
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GenotypeQuality
all individuals: 1320
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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: 391
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16056
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66174
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

FS
type: SiteQuality
SIO_000300: 4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.898e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.284e1

MQRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.49e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.700199e6

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

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.25e1
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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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
all individuals: 38
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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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3922
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.233636703652911e-5
allele num: 16042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66150
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.662e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-1

FS
type: SiteQuality
SIO_000300: 1.1347e1

QD
type: SiteQuality
SIO_000300: 1.224e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

DP
type: SiteQuality
SIO_000300: 1.699292e6

GenotypeQuality
all individuals: 45450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5040
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.544077552256892e-4
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65978
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

DP
type: SiteQuality
SIO_000300: 1.6923e6

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.279e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
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GenotypeQuality
all individuals: 1783
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 579
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55048375093029e-5
allele num: 64496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.609151e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 2.079e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 9.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e-1

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 2.75e1
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GenotypeQuality
all individuals: 1226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
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GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 311
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GenotypeQuality
all individuals: 2340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14676
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64166
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.192179303767287e-4
allele num: 8388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.586e6

QD
type: SiteQuality
SIO_000300: 7.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

GenotypeQuality
all individuals: 32270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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: 3.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.1312625250501e-5
allele num: 63872
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.712e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

DP
type: SiteQuality
SIO_000300: 1.552787e6

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 520
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.254390366281987e-4
allele num: 63776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.99000999000999e-5
allele num: 10010
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 1.547528e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 2.222e0

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 108

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63522
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.181184668989547e-4
allele num: 14350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.162790697674419e-3
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 104
allele frequency: 1.256342111621165e-2
allele num: 8278
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.29e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e0

DP
type: SiteQuality
SIO_000300: 1.517339e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 16

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.22667557336896e-4
allele num: 62874
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.979885057471264e-5
allele num: 11136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13906
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.010305112143867e-4
allele num: 9898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

DP
type: SiteQuality
SIO_000300: 1.447317e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1040
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GenotypeQuality
all individuals: 3910
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.607820438613416e-5
allele num: 62196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8040
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.395784e6

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.94e-1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

GenotypeQuality
all individuals: 808
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7415
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628929793125916e-5
allele num: 61390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.493e0

DP
type: SiteQuality
SIO_000300: 1.370461e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeQuality
all individuals: 3364
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variant carriers: 0

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

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: 7954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.562008469449486e-5
allele num: 13224
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.493e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 1.370461e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 449
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 1.681143177360605e-3
allele num: 7138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.078e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

DP
type: SiteQuality
SIO_000300: 8.59212e5

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

QD
type: SiteQuality
SIO_000300: 1.502e1

GenotypeQuality
all individuals: 1649
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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
all individuals: 1606
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GenotypeQuality
all individuals: 2106
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097755401720159e-5
allele num: 47670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.431e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.78155e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
all individuals: 9139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
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GenotypeQuality
all individuals: 1062
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GenotypeQuality
all individuals: 558
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 34937
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57172
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.97561622051418e-4
allele num: 7546
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.254e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 1.240285e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.84e-1

FS
type: SiteQuality
SIO_000300: 4.579e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

GenotypeQuality
all individuals: 550
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8601
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35947
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.447919180774402e-5
allele num: 58006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 1.254918e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.19e1

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.377579626439694e-5
allele num: 59214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.279274e6

FS
type: SiteQuality
SIO_000300: 8.19e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60000
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.187798603454613e-5
allele num: 10884
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.120071684587814e-4
allele num: 8928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.755e0

QD
type: SiteQuality
SIO_000300: 1.119e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.295549e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

GenotypeQuality
all individuals: 438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1179
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21300339640951e-4
allele num: 8244
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.326796e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.541e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40084
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 153
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10846
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.091e0

DP
type: SiteQuality
SIO_000300: 1.341434e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.706e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.815232722143864e-5
allele num: 11344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.753002313127793e-5
allele num: 63118
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.566295979469632e-4
allele num: 11690
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 8.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

DP
type: SiteQuality
SIO_000300: 1.358571e6

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: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63650
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173158141717503e-4
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 4.89e0

FS
type: SiteQuality
SIO_000300: 2.859e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.371267e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.617e0

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
all individuals: 1981
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GenotypeQuality
all individuals: 526
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558700667123886e-5
allele num: 64156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12984
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.963e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.516e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 1.383151e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.838393274170948e-4
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64354
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

DP
type: SiteQuality
SIO_000300: 1.389797e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.51e0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

FS
type: SiteQuality
SIO_000300: 4.425e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 1.026e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
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: 64530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.682e0

QD
type: SiteQuality
SIO_000300: 1.089e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

DP
type: SiteQuality
SIO_000300: 1.395284e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.796e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1823
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2054
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variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.732193348592971e-5
allele num: 14854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65220
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

DP
type: SiteQuality
SIO_000300: 1.415339e6

VQSLOD
type: SiteQuality
SIO_000300: -8.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.82e-1

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 1819
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
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: 0
allele frequency: 0.0e0
allele num: 65336
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

FS
type: SiteQuality
SIO_000300: 4.026e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

DP
type: SiteQuality
SIO_000300: 1.418487e6

GenotypeQuality
all individuals: 5881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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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: 18
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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: 1785
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65516
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: 15346
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.476e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 2.847e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

DP
type: SiteQuality
SIO_000300: 1.425444e6

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 1792
bin: 9.75e1
variant carriers: 1

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: 2
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 550
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variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 1.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.447931e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.091e0

QD
type: SiteQuality
SIO_000300: 1.433e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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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
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
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: 11526
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.496e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.448767e6

QD
type: SiteQuality
SIO_000300: 9.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.904e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.03e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 27
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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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
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variant carriers: 0

GenotypeQuality
all individuals: 45398
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 17
allele frequency: 1.034189074096605e-3
allele num: 16438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 1.451289e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.681e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.259e1

FS
type: SiteQuality
SIO_000300: 5.96e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 434
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.055552204596176e-4
allele num: 66316
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: 8.59e-1

DP
type: SiteQuality
SIO_000300: 1.45151e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
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South Asian
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allele num: 16468
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66364
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Latino
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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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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African
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allele num: 10154
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.51222813825467e-5
allele num: 66486
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African
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QD
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InbreedingCoeff
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MQ
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DP
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FS
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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allele frequency: 0.0e0
allele num: 906
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.658008658008658e-5
allele num: 11550
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East Asian
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African
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FS
type: SiteQuality
SIO_000300: 7.95e-1

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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allele num: 6612
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South Asian
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Other
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ReadPosRankSum
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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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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variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

African
type: Population
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allele frequency: 9.852216748768474e-5
allele num: 10150
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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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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Latino
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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African
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East Asian
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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East Asian
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VQSLOD
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DP
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QD
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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DP
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MQ
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VQSLOD
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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
all individuals: 1940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2181
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.427e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 1.449378e6

GenotypeQuality
all individuals: 1408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2181
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
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: 10084
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.097e0

QD
type: SiteQuality
SIO_000300: 1.217e1

FS
type: SiteQuality
SIO_000300: 1.2558e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.44735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2371
bin: 9.75e1
variant carriers: 598

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

Latino
type: Population
allele count: 46
allele frequency: 3.990976921742148e-3
allele num: 11526
num of homozygotes: 1

African
type: Population
allele count: 508
allele frequency: 5.037683458944863e-2
allele num: 10084
num of homozygotes: 13

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

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

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 8.748378533289089e-4
allele num: 66298
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.484303e6

QD
type: SiteQuality
SIO_000300: 1.347e1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.727e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.59e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

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

GenotypeQuality
all individuals: 2012
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 7.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.621e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.171e0

DP
type: SiteQuality
SIO_000300: 1.456496e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.592e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 1.038e0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.932459276916965e-5
allele num: 10068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.03554938588285e-5
allele num: 66274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

DP
type: SiteQuality
SIO_000300: 1.456531e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.209e1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.385e0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
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: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.306e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e0

FS
type: SiteQuality
SIO_000300: 1.4607e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

DP
type: SiteQuality
SIO_000300: 1.455766e6

QD
type: SiteQuality
SIO_000300: 1.366e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.77e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 6015
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 659
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.736111111111111e-4
allele num: 11520
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

DP
type: SiteQuality
SIO_000300: 1.455394e6

FS
type: SiteQuality
SIO_000300: 5.481e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e-1

GenotypeQuality
all individuals: 6017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.529669334138608e-5
allele num: 66230
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.455321e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.377e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2018
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21447656060238e-4
allele num: 16468
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: 10060
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

FS
type: SiteQuality
SIO_000300: 5.652e0

DP
type: SiteQuality
SIO_000300: 1.455207e6

QD
type: SiteQuality
SIO_000300: 1.206e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

GenotypeQuality
all individuals: 587
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1428
bin: 8.25e1
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: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021695775669306e-5
allele num: 66188
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.493e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 1.454199e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e0

FS
type: SiteQuality
SIO_000300: 1.441e0

VQSLOD
type: SiteQuality
SIO_000300: 6.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
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
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.453815e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

QD
type: SiteQuality
SIO_000300: 1.499e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43718
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.972078181092939e-5
allele num: 10028
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: 8628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66096
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.391e1

FS
type: SiteQuality
SIO_000300: 6.062e0

DP
type: SiteQuality
SIO_000300: 1.453282e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
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: 11510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513134003147319e-5
allele num: 66088
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.116e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

DP
type: SiteQuality
SIO_000300: 1.453521e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
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: 10028
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.344048653344917e-4
allele num: 11510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66092
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.206e0

MQ
type: SiteQuality
SIO_000300: 5.581e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.453727e6

QD
type: SiteQuality
SIO_000300: 1.689e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.72e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43675
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.988014382740711e-5
allele num: 10012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.456042e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

QD
type: SiteQuality
SIO_000300: 1.332e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.966e0

GenotypeQuality
all individuals: 703
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6103
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.162e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.129e0

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

DP
type: SiteQuality
SIO_000300: 1.456398e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
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variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.984025559105431e-5
allele num: 10016
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66052
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.434e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.78e-1

QD
type: SiteQuality
SIO_000300: 1.656e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.271e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 1.456994e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.570710435467265e-5
allele num: 66044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.457531e6

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 1.505e1

FS
type: SiteQuality
SIO_000300: 2.465e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43702
bin: 6.25e1
variant carriers: 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: 11510
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: 898
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513546238837597e-5
allele num: 66070
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 1.459313e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.252e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.899e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513500423780119e-5
allele num: 66072
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.459944e6

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43718
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: -1.137e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.357e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.177e0

VQSLOD
type: SiteQuality
SIO_000300: -2.861e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.460257e6

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeQuality
all individuals: 2265
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027275754548482e-5
allele num: 66066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.60778859527121e-4
allele num: 11504
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.733e0

QD
type: SiteQuality
SIO_000300: 1.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.46331e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43531
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738525730180807e-4
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.000400080016003e-4
allele num: 9998
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.724548179093634e-4
allele num: 66066
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.036929057337221e-4
allele num: 16464
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.733e0

QD
type: SiteQuality
SIO_000300: 1.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.46331e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 1479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 696
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027550711474417e-5
allele num: 66060
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

DP
type: SiteQuality
SIO_000300: 1.463419e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.418e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.511e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513454611496201e-5
allele num: 66074
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
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: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.188e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

DP
type: SiteQuality
SIO_000300: 1.463712e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

GenotypeQuality
all individuals: 43559
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.214771622934888e-4
allele num: 16464
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.463718e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.222e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

GenotypeQuality
all individuals: 2302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43538
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 1.463774e6

VQSLOD
type: SiteQuality
SIO_000300: -5.798e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 9.895e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.037e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1