19-38230312-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230312
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230312
    reference: chr 19
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.815G>A
  hgvsp: ENSP00000349861.3:p.Cys272Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.815G>A
  hgvsp: ENSP00000440464.1:p.Cys272Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1079G>A
  hgvsp: ENSP00000465020.1:p.Cys360Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*960G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*955G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.818G>A
  hgvsp: ENSP00000375983.1:p.Cys273Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+673G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.905G>A
  hgvsp: ENSP00000340171.4:p.Cys302Tyr
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20679
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6644
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22719
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys360Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-38230321-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230321
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230321
    reference: chr 19
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1070C>A
  hgvsp: ENSP00000465020.1:p.Pro357His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.809C>A
  hgvsp: ENSP00000375983.1:p.Pro270His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.806C>A
  hgvsp: ENSP00000440464.1:p.Pro269His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+664C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.896C>A
  hgvsp: ENSP00000340171.4:p.Pro299His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*946C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.806C>A
  hgvsp: ENSP00000349861.3:p.Pro269His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*951C>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro357His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-38230336-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230336
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230336
    reference: chr 19
allele count: 2
allele frequency: 1.651418568550385e-5
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.791A>G
  hgvsp: ENSP00000349861.3:p.His264Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1055A>G
  hgvsp: ENSP00000465020.1:p.His352Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.881A>G
  hgvsp: ENSP00000340171.4:p.His294Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*936A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.791A>G
  hgvsp: ENSP00000440464.1:p.His264Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*931A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.794A>G
  hgvsp: ENSP00000375983.1:p.His265Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+649A>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His352Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-38230336-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230336
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230336
    reference: chr 19
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.791A>C
  hgvsp: ENSP00000440464.1:p.His264Pro
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.791A>C
  hgvsp: ENSP00000349861.3:p.His264Pro
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*931A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+649A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1055A>C
  hgvsp: ENSP00000465020.1:p.His352Pro
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.881A>C
  hgvsp: ENSP00000340171.4:p.His294Pro
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*936A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.794A>C
  hgvsp: ENSP00000375983.1:p.His265Pro
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22642
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His352Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

19-38230348-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230348
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230348
    reference: chr 19
allele count: 7
allele frequency: 5.780824180361715e-5
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+637A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1043A>G
  hgvsp: ENSP00000465020.1:p.His348Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.779A>G
  hgvsp: ENSP00000349861.3:p.His260Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.869A>G
  hgvsp: ENSP00000340171.4:p.His290Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.779A>G
  hgvsp: ENSP00000440464.1:p.His260Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.782A>G
  hgvsp: ENSP00000375983.1:p.His261Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*919A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*924A>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17088
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His348Arg
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

19-38230349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230349
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230349
    reference: chr 19
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.778C>T
  hgvsp: ENSP00000349861.3:p.His260Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.781C>T
  hgvsp: ENSP00000375983.1:p.His261Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.778C>T
  hgvsp: ENSP00000440464.1:p.His260Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+636C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*923C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1042C>T
  hgvsp: ENSP00000465020.1:p.His348Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.868C>T
  hgvsp: ENSP00000340171.4:p.His290Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*918C>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His348Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

19-38230356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230356
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230356
    reference: chr 19
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.774T>C
  hgvsp: ENST00000392138.1:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.771T>C
  hgvsp: ENST00000357309.3:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.861T>C
  hgvsp: ENST00000339503.4:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*911T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+629T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1035T>C
  hgvsp: ENST00000590414.2:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.771T>C
  hgvsp: ENST00000536220.1:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*916T>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe345Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-38230358-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230358
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230358
    reference: chr 19
allele count: 3
allele frequency: 2.478847170809096e-5
allele num: 121024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.769T>G
  hgvsp: ENSP00000440464.1:p.Phe257Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1033T>G
  hgvsp: ENSP00000465020.1:p.Phe345Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*909T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+627T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.769T>G
  hgvsp: ENSP00000349861.3:p.Phe257Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*914T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.772T>G
  hgvsp: ENSP00000375983.1:p.Phe258Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.859T>G
  hgvsp: ENSP00000340171.4:p.Phe287Val
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe345Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-38230365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230365
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230365
    reference: chr 19
allele count: 28
allele frequency: 2.313858358813321e-4
allele num: 121010
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1026C>T
  hgvsp: ENST00000590414.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+620C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.765C>T
  hgvsp: ENST00000392138.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.762C>T
  hgvsp: ENST00000536220.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.852C>T
  hgvsp: ENST00000339503.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.762C>T
  hgvsp: ENST00000357309.3:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*907C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*902C>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 17000
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala342Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/19-38230376-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230376
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230376
    reference: chr 19
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.754T>G
  hgvsp: ENSP00000375983.1:p.Tyr252Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+609T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*896T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1015T>G
  hgvsp: ENSP00000465020.1:p.Tyr339Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.751T>G
  hgvsp: ENSP00000349861.3:p.Tyr251Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.841T>G
  hgvsp: ENSP00000340171.4:p.Tyr281Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.751T>G
  hgvsp: ENSP00000440464.1:p.Tyr251Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*891T>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr339Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

19-38230384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230384
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230384
    reference: chr 19
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+601G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.1007G>A
  hgvsp: ENSP00000465020.1:p.Gly336Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.833G>A
  hgvsp: ENSP00000340171.4:p.Gly278Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.743G>A
  hgvsp: ENSP00000440464.1:p.Gly248Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*888G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.743G>A
  hgvsp: ENSP00000349861.3:p.Gly248Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*883G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.746G>A
  hgvsp: ENSP00000375983.1:p.Gly249Glu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly336Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

19-38230396-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230396
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230396
    reference: chr 19
allele count: 2
allele frequency: 1.655437283758505e-5
allele num: 120814
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.995G>A
  hgvsp: ENSP00000465020.1:p.Cys332Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.734G>A
  hgvsp: ENSP00000375983.1:p.Cys245Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.821G>A
  hgvsp: ENSP00000340171.4:p.Cys274Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+589G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*876G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*871G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.731G>A
  hgvsp: ENSP00000349861.3:p.Cys244Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.731G>A
  hgvsp: ENSP00000440464.1:p.Cys244Tyr
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys332Tyr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

19-38230423-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230423
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230421
    reference: chr 19
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.705_706delAG
  hgvsp: ENSP00000375983.1:p.Arg235SerfsTer5
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.702_703delAG
  hgvsp: ENSP00000440464.1:p.Arg234SerfsTer5
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.702_703delAG
  hgvsp: ENSP00000349861.3:p.Arg234SerfsTer5
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*842_*843delAG
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.966_967delAG
  hgvsp: ENSP00000465020.1:p.Arg322SerfsTer5
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.792_793delAG
  hgvsp: ENSP00000340171.4:p.Arg264SerfsTer5
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*847_*848delAG
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+560_55+561delAG
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20664
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg322SerfsTer5
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: ACT
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-38230430-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230430
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230430
    reference: chr 19
allele count: 4
allele frequency: 3.314001657000828e-5
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*842C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.697C>A
  hgvsp: ENSP00000440464.1:p.Gln233Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.700C>A
  hgvsp: ENSP00000375983.1:p.Gln234Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+555C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*837C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.961C>A
  hgvsp: ENSP00000465020.1:p.Gln321Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.697C>A
  hgvsp: ENSP00000349861.3:p.Gln233Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.787C>A
  hgvsp: ENSP00000340171.4:p.Gln263Lys
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20678
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln321Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

19-38230433-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230433
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230433
    reference: chr 19
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.784C>T
  hgvsp: ENSP00000340171.4:p.His262Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.694C>T
  hgvsp: ENSP00000349861.3:p.His232Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*834C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.697C>T
  hgvsp: ENSP00000375983.1:p.His233Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.958C>T
  hgvsp: ENSP00000465020.1:p.His320Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*839C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.694C>T
  hgvsp: ENSP00000440464.1:p.His232Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+552C>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His320Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

19-38230434-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230434
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230434
    reference: chr 19
allele count: 13
allele frequency: 1.076997000977582e-4
allele num: 120706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*838A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.957A>T
  hgvsp: ENST00000590414.2:c.957A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.693A>T
  hgvsp: ENST00000357309.3:c.693A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.783A>T
  hgvsp: ENST00000339503.4:c.783A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*833A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.693A>T
  hgvsp: ENST00000536220.1:c.693A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.696A>T
  hgvsp: ENST00000392138.1:c.696A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+551A>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6313
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val319Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS

19-38230437-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230437
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230437
    reference: chr 19
allele count: 13
allele frequency: 1.076836420264405e-4
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.954T>A
  hgvsp: ENST00000590414.2:c.954T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.690T>A
  hgvsp: ENST00000357309.3:c.690T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+548T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*830T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.780T>A
  hgvsp: ENST00000339503.4:c.780T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.693T>A
  hgvsp: ENST00000392138.1:c.693T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.690T>A
  hgvsp: ENST00000536220.1:c.690T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*835T>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6305
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr318Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-38230438-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230438
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230438
    reference: chr 19
allele count: 13
allele frequency: 1.077300450808804e-4
allele num: 120672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.689C>G
  hgvsp: ENSP00000440464.1:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+547C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.953C>G
  hgvsp: ENSP00000465020.1:p.Thr318Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.692C>G
  hgvsp: ENSP00000375983.1:p.Thr231Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*834C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*829C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.779C>G
  hgvsp: ENSP00000340171.4:p.Thr260Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.689C>G
  hgvsp: ENSP00000349861.3:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr318Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

19-38230439-TAAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230439
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230436
    reference: chr 19
allele count: 13
allele frequency: 1.077121930202499e-4
allele num: 120692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.685_687delCTT
  hgvsp: ENSP00000440464.1:p.Leu229del
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.775_777delCTT
  hgvsp: ENSP00000340171.4:p.Leu259del
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+543_55+545delCTT
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.688_690delCTT
  hgvsp: ENSP00000375983.1:p.Leu230del
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*825_*827delCTT
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.685_687delCTT
  hgvsp: ENSP00000349861.3:p.Leu229del
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*830_*832delCTT
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.949_951delCTT
  hgvsp: ENSP00000465020.1:p.Leu317del
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20567
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu317del
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: TAAG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

19-38230450-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230450
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230450
    reference: chr 19
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*822G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.680G>C
  hgvsp: ENSP00000375983.1:p.Gly227Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.677G>C
  hgvsp: ENSP00000440464.1:p.Gly226Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.677G>C
  hgvsp: ENSP00000349861.3:p.Gly226Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.767G>C
  hgvsp: ENSP00000340171.4:p.Gly256Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.941G>C
  hgvsp: ENSP00000465020.1:p.Gly314Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*817G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+535G>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20659
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly314Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

19-38230451-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230451
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230451
    reference: chr 19
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.676G>C
  hgvsp: ENSP00000349861.3:p.Gly226Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.766G>C
  hgvsp: ENSP00000340171.4:p.Gly256Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*816G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+534G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.676G>C
  hgvsp: ENSP00000440464.1:p.Gly226Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*821G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.940G>C
  hgvsp: ENSP00000465020.1:p.Gly314Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.679G>C
  hgvsp: ENSP00000375983.1:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly314Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

19-38230474-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230474
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230474
    reference: chr 19
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.917A>G
  hgvsp: ENSP00000465020.1:p.Lys306Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.656A>G
  hgvsp: ENSP00000375983.1:p.Lys219Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+511A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.743A>G
  hgvsp: ENSP00000340171.4:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*793A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*798A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.653A>G
  hgvsp: ENSP00000440464.1:p.Lys218Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.653A>G
  hgvsp: ENSP00000349861.3:p.Lys218Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2917
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22073
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys306Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS

19-38230481-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230481
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230481
    reference: chr 19
allele count: 2
allele frequency: 1.653931394925738e-5
allele num: 120924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.649T>C
  hgvsp: ENSP00000375983.1:p.Cys217Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.646T>C
  hgvsp: ENSP00000349861.3:p.Cys216Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.910T>C
  hgvsp: ENSP00000465020.1:p.Cys304Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*786T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+504T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*791T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.736T>C
  hgvsp: ENSP00000340171.4:p.Cys246Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.646T>C
  hgvsp: ENSP00000440464.1:p.Cys216Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20658
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys304Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

19-38230487-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230487
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230487
    reference: chr 19
allele count: 2
allele frequency: 1.653302471687195e-5
allele num: 120970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.730T>A
  hgvsp: ENSP00000340171.4:p.Tyr244Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.640T>A
  hgvsp: ENSP00000440464.1:p.Tyr214Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*785T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.643T>A
  hgvsp: ENSP00000375983.1:p.Tyr215Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.904T>A
  hgvsp: ENSP00000465020.1:p.Tyr302Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+498T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*780T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.640T>A
  hgvsp: ENSP00000349861.3:p.Tyr214Asn
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16317
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr302Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-38230491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230491
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230491
    reference: chr 19
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.636G>A
  hgvsp: ENST00000536220.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.726G>A
  hgvsp: ENST00000339503.4:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*781G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*776G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+494G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.639G>A
  hgvsp: ENST00000392138.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.900G>A
  hgvsp: ENST00000590414.2:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.636G>A
  hgvsp: ENST00000357309.3:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys300Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-38230494-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230494
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230494
    reference: chr 19
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.723G>C
  hgvsp: ENSP00000340171.4:p.Glu241Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.636G>C
  hgvsp: ENSP00000375983.1:p.Glu212Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.633G>C
  hgvsp: ENSP00000440464.1:p.Glu211Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.897G>C
  hgvsp: ENSP00000465020.1:p.Glu299Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.633G>C
  hgvsp: ENSP00000349861.3:p.Glu211Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+491G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*778G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*773G>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu299Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

19-38230497-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230497
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230497
    reference: chr 19
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+488T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.894T>A
  hgvsp: ENSP00000465020.1:p.Asp298Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*775T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*770T>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.633T>A
  hgvsp: ENSP00000375983.1:p.Asp211Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.630T>A
  hgvsp: ENSP00000440464.1:p.Asp210Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.720T>A
  hgvsp: ENSP00000340171.4:p.Asp240Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.630T>A
  hgvsp: ENSP00000349861.3:p.Asp210Glu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp298Glu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-38230503-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230503
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230503
    reference: chr 19
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+482T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.714T>C
  hgvsp: ENST00000339503.4:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.627T>C
  hgvsp: ENST00000392138.1:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.624T>C
  hgvsp: ENST00000357309.3:c.624T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*764T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.888T>C
  hgvsp: ENST00000590414.2:c.888T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.624T>C
  hgvsp: ENST00000536220.1:c.624T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*769T>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His296His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

19-38230512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230512
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230512
    reference: chr 19
allele count: 3
allele frequency: 2.47618733182561e-5
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.705G>A
  hgvsp: ENST00000339503.4:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.615G>A
  hgvsp: ENST00000357309.3:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.615G>A
  hgvsp: ENST00000536220.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*755G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+473G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.618G>A
  hgvsp: ENST00000392138.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*760G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.879G>A
  hgvsp: ENST00000590414.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20658
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly293Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

19-38230526-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230526
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230526
    reference: chr 19
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.691C>G
  hgvsp: ENSP00000340171.4:p.Leu231Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.865C>G
  hgvsp: ENSP00000465020.1:p.Leu289Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.601C>G
  hgvsp: ENSP00000440464.1:p.Leu201Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+459C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.604C>G
  hgvsp: ENSP00000375983.1:p.Leu202Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*741C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.601C>G
  hgvsp: ENSP00000349861.3:p.Leu201Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*746C>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu289Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

19-38230528-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230528
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230528
    reference: chr 19
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.689A>G
  hgvsp: ENSP00000340171.4:p.Asn230Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.599A>G
  hgvsp: ENSP00000440464.1:p.Asn200Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.863A>G
  hgvsp: ENSP00000465020.1:p.Asn288Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+457A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.599A>G
  hgvsp: ENSP00000349861.3:p.Asn200Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*744A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.602A>G
  hgvsp: ENSP00000375983.1:p.Asn201Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*739A>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn288Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-38230534-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230534
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230534
    reference: chr 19
allele count: 79
allele frequency: 6.51600131969647e-4
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.683G>A
  hgvsp: ENSP00000340171.4:p.Arg228His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.857G>A
  hgvsp: ENSP00000465020.1:p.Arg286His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+451G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.593G>A
  hgvsp: ENSP00000349861.3:p.Arg198His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*733G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.593G>A
  hgvsp: ENSP00000440464.1:p.Arg198His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.596G>A
  hgvsp: ENSP00000375983.1:p.Arg199His
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16586
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 9.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg286His
num of homozygotes: 1
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

19-38230535-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230535
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230535
    reference: chr 19
allele count: 13
allele frequency: 1.072218006664247e-4
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.856C>T
  hgvsp: ENSP00000465020.1:p.Arg286Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.682C>T
  hgvsp: ENSP00000340171.4:p.Arg228Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*737C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+450C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.592C>T
  hgvsp: ENSP00000440464.1:p.Arg198Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*732C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.595C>T
  hgvsp: ENSP00000375983.1:p.Arg199Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.592C>T
  hgvsp: ENSP00000349861.3:p.Arg198Cys
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20617
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg286Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-38230537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230537
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230537
    reference: chr 19
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.590G>A
  hgvsp: ENSP00000440464.1:p.Arg197Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+448G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*735G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.593G>A
  hgvsp: ENSP00000375983.1:p.Arg198Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.854G>A
  hgvsp: ENSP00000465020.1:p.Arg285Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.680G>A
  hgvsp: ENSP00000340171.4:p.Arg227Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.590G>A
  hgvsp: ENSP00000349861.3:p.Arg197Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*730G>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg285Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-38230540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230540
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230540
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.590G>A
  hgvsp: ENSP00000375983.1:p.Ser197Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.587G>A
  hgvsp: ENSP00000440464.1:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.851G>A
  hgvsp: ENSP00000465020.1:p.Ser284Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*732G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*727G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.587G>A
  hgvsp: ENSP00000349861.3:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.677G>A
  hgvsp: ENSP00000340171.4:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+445G>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6514
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser284Asn
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

19-38230544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230544
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230544
    reference: chr 19
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.847T>C
  hgvsp: ENSP00000465020.1:p.Phe283Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*723T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+441T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*728T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.583T>C
  hgvsp: ENSP00000440464.1:p.Phe195Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.583T>C
  hgvsp: ENSP00000349861.3:p.Phe195Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.586T>C
  hgvsp: ENSP00000375983.1:p.Phe196Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.673T>C
  hgvsp: ENSP00000340171.4:p.Phe225Leu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20609
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe283Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

19-38230571-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230571
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230571
    reference: chr 19
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.646T>C
  hgvsp: ENSP00000340171.4:p.Tyr216His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+414T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.820T>C
  hgvsp: ENSP00000465020.1:p.Tyr274His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.556T>C
  hgvsp: ENSP00000440464.1:p.Tyr186His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.556T>C
  hgvsp: ENSP00000349861.3:p.Tyr186His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*696T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.559T>C
  hgvsp: ENSP00000375983.1:p.Tyr187His
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22638
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr274His
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

19-38230572-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230572
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230572
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.819A>G
  hgvsp: ENST00000590414.2:c.819A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.555A>G
  hgvsp: ENST00000357309.3:c.555A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+413A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.558A>G
  hgvsp: ENST00000392138.1:c.558A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*695A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.645A>G
  hgvsp: ENST00000339503.4:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.555A>G
  hgvsp: ENST00000536220.1:c.555A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*700A>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro273Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

19-38230580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230580
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230580
    reference: chr 19
allele count: 3
allele frequency: 2.474594166556685e-5
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.547G>A
  hgvsp: ENSP00000349861.3:p.Glu183Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.637G>A
  hgvsp: ENSP00000340171.4:p.Glu213Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.550G>A
  hgvsp: ENSP00000375983.1:p.Glu184Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.547G>A
  hgvsp: ENSP00000440464.1:p.Glu183Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.811G>A
  hgvsp: ENSP00000465020.1:p.Glu271Lys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*687G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*692G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+405G>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu271Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

19-38230581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230581
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230581
    reference: chr 19
allele count: 1253
allele frequency: 1.03377720574889e-2
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.546C>T
  hgvsp: ENST00000357309.3:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.549C>T
  hgvsp: ENST00000392138.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.810C>T
  hgvsp: ENST00000590414.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*686C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.546C>T
  hgvsp: ENST00000536220.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*691C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.636C>T
  hgvsp: ENST00000339503.4:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+404C>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16248
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 9.75e1
  variant carriers: 802
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly270Gly
num of homozygotes: 12
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

19-38230585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230585
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230585
    reference: chr 19
allele count: 19
allele frequency: 1.567113706471355e-4
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.806C>T
  hgvsp: ENSP00000465020.1:p.Thr269Ile
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.542C>T
  hgvsp: ENSP00000349861.3:p.Thr181Ile
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+400C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.545C>T
  hgvsp: ENSP00000375983.1:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*682C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.542C>T
  hgvsp: ENSP00000440464.1:p.Thr181Ile
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.632C>T
  hgvsp: ENSP00000340171.4:p.Thr211Ile
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*687C>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2188
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr269Ile
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-38230605-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230605
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230605
    reference: chr 19
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.525A>T
  hgvsp: ENSP00000375983.1:p.Arg175Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.612A>T
  hgvsp: ENSP00000340171.4:p.Arg204Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+380A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.522A>T
  hgvsp: ENSP00000349861.3:p.Arg174Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*662A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.522A>T
  hgvsp: ENSP00000440464.1:p.Arg174Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*667A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.786A>T
  hgvsp: ENSP00000465020.1:p.Arg262Ser
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16291
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20015
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg262Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP

19-38230610-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230610
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230610
    reference: chr 19
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.517C>G
  hgvsp: ENSP00000349861.3:p.Leu173Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.520C>G
  hgvsp: ENSP00000375983.1:p.Leu174Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.517C>G
  hgvsp: ENSP00000440464.1:p.Leu173Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*657C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.607C>G
  hgvsp: ENSP00000340171.4:p.Leu203Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+375C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*662C>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.781C>G
  hgvsp: ENSP00000465020.1:p.Leu261Val
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20016
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu261Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

19-38230610-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230610
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230609
    reference: chr 19
allele count: 3
allele frequency: 2.47537006782514e-5
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+374delT
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.606delT
  hgvsp: ENSP00000340171.4:p.Arg204GlufsTer178
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*661delT
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.519delT
  hgvsp: ENSP00000375983.1:p.Arg175GlufsTer178
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.516delT
  hgvsp: ENSP00000349861.3:p.Arg174GlufsTer178
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.516delT
  hgvsp: ENSP00000440464.1:p.Arg174GlufsTer178
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.780delT
  hgvsp: ENSP00000465020.1:p.Arg262GlufsTer178
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*656delT
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20016
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg262GlufsTer178
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: GA
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

19-38230616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230616
    reference: chr 19
allele count: 2
allele frequency: 1.650955077512341e-5
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*651G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.775G>A
  hgvsp: ENSP00000465020.1:p.Gly259Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.511G>A
  hgvsp: ENSP00000440464.1:p.Gly171Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*656G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+369G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.601G>A
  hgvsp: ENSP00000340171.4:p.Gly201Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.511G>A
  hgvsp: ENSP00000349861.3:p.Gly171Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.514G>A
  hgvsp: ENSP00000375983.1:p.Gly172Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16255
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22090
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly259Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-38230623-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230623
    reference: chr 19
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*649T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.504T>G
  hgvsp: ENSP00000349861.3:p.Ser168Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.504T>G
  hgvsp: ENSP00000440464.1:p.Ser168Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.594T>G
  hgvsp: ENSP00000340171.4:p.Ser198Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+362T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.768T>G
  hgvsp: ENSP00000465020.1:p.Ser256Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*644T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.507T>G
  hgvsp: ENSP00000375983.1:p.Ser169Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6523
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser256Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-38230627-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230627
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230627
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*640T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+358T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.764T>C
  hgvsp: ENSP00000465020.1:p.Phe255Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*645T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.503T>C
  hgvsp: ENSP00000375983.1:p.Phe168Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.500T>C
  hgvsp: ENSP00000349861.3:p.Phe167Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.590T>C
  hgvsp: ENSP00000340171.4:p.Phe197Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.500T>C
  hgvsp: ENSP00000440464.1:p.Phe167Ser
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22349
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe255Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

19-38230628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230628
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230628
    reference: chr 19
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*639T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.499T>C
  hgvsp: ENSP00000440464.1:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.502T>C
  hgvsp: ENSP00000375983.1:p.Phe168Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.589T>C
  hgvsp: ENSP00000340171.4:p.Phe197Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.763T>C
  hgvsp: ENSP00000465020.1:p.Phe255Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.499T>C
  hgvsp: ENSP00000349861.3:p.Phe167Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+357T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*644T>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20011
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe255Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-38230648-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230648
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230648
    reference: chr 19
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.569G>A
  hgvsp: ENSP00000340171.4:p.Cys190Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.482G>A
  hgvsp: ENSP00000375983.1:p.Cys161Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*619G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.479G>A
  hgvsp: ENSP00000440464.1:p.Cys160Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*624G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+337G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.743G>A
  hgvsp: ENSP00000465020.1:p.Cys248Tyr
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.479G>A
  hgvsp: ENSP00000349861.3:p.Cys160Tyr
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys248Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

19-38230653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230653
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230653
    reference: chr 19
allele count: 3
allele frequency: 2.474063566939913e-5
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*619T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.474T>C
  hgvsp: ENST00000536220.1:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.738T>C
  hgvsp: ENST00000590414.2:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.564T>C
  hgvsp: ENST00000339503.4:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.474T>C
  hgvsp: ENST00000357309.3:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.477T>C
  hgvsp: ENST00000392138.1:c.477T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*614T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+332T>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr246Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

19-38230654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230654
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230654
    reference: chr 19
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.737A>G
  hgvsp: ENSP00000465020.1:p.Tyr246Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+331A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*618A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.473A>G
  hgvsp: ENSP00000440464.1:p.Tyr158Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.473A>G
  hgvsp: ENSP00000349861.3:p.Tyr158Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.563A>G
  hgvsp: ENSP00000340171.4:p.Tyr188Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.476A>G
  hgvsp: ENSP00000375983.1:p.Tyr159Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*613A>G
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr246Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

19-38230656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230656
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230656
    reference: chr 19
allele count: 37
allele frequency: 3.051949123183265e-4
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.471G>A
  hgvsp: ENST00000536220.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*616G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.471G>A
  hgvsp: ENST00000357309.3:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.474G>A
  hgvsp: ENST00000392138.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.561G>A
  hgvsp: ENST00000339503.4:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.735G>A
  hgvsp: ENST00000590414.2:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*611G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+329G>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro245Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

19-38230657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230657
    reference: chr 19
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.734C>T
  hgvsp: ENSP00000465020.1:p.Pro245Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.470C>T
  hgvsp: ENSP00000349861.3:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.470C>T
  hgvsp: ENSP00000440464.1:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*610C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*615C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+328C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.560C>T
  hgvsp: ENSP00000340171.4:p.Pro187Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.473C>T
  hgvsp: ENSP00000375983.1:p.Pro158Leu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20002
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro245Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-38230661-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230661
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230661
    reference: chr 19
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.556A>T
  hgvsp: ENSP00000340171.4:p.Lys186Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.466A>T
  hgvsp: ENSP00000349861.3:p.Lys156Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*606A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.469A>T
  hgvsp: ENSP00000375983.1:p.Lys157Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.466A>T
  hgvsp: ENSP00000440464.1:p.Lys156Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.730A>T
  hgvsp: ENSP00000465020.1:p.Lys244Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+324A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*611A>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys244Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

19-38230671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230671
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230671
    reference: chr 19
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.456C>T
  hgvsp: ENST00000357309.3:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.546C>T
  hgvsp: ENST00000339503.4:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.459C>T
  hgvsp: ENST00000392138.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*596C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+314C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.720C>T
  hgvsp: ENST00000590414.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*601C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.456C>T
  hgvsp: ENST00000536220.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1607
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His240His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-38230676-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230676
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230676
    reference: chr 19
allele count: 3
allele frequency: 2.47255464345762e-5
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.451A>G
  hgvsp: ENSP00000440464.1:p.Ile151Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.541A>G
  hgvsp: ENSP00000340171.4:p.Ile181Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*596A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.451A>G
  hgvsp: ENSP00000349861.3:p.Ile151Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.454A>G
  hgvsp: ENSP00000375983.1:p.Ile152Val
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*591A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+309A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.715A>G
  hgvsp: ENSP00000465020.1:p.Ile239Val
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23357
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile239Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-38230682-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230682
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230682
    reference: chr 19
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.445G>T
  hgvsp: ENSP00000440464.1:p.Glu149Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*585G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*590G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+303G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.709G>T
  hgvsp: ENSP00000465020.1:p.Glu237Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.535G>T
  hgvsp: ENSP00000340171.4:p.Glu179Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.445G>T
  hgvsp: ENSP00000349861.3:p.Glu149Ter
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.448G>T
  hgvsp: ENSP00000375983.1:p.Glu150Ter
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20011
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6678
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu237Ter
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

19-38230691-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230691
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230691
    reference: chr 19
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.436G>C
  hgvsp: ENSP00000440464.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*581G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.700G>C
  hgvsp: ENSP00000465020.1:p.Val234Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*576G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.439G>C
  hgvsp: ENSP00000375983.1:p.Val147Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.436G>C
  hgvsp: ENSP00000349861.3:p.Val146Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+294G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.526G>C
  hgvsp: ENSP00000340171.4:p.Val176Leu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20010
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23440
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val234Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-38230695-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230695
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230695
    reference: chr 19
allele count: 18
allele frequency: 1.483288285318742e-4
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.696C>A
  hgvsp: ENSP00000465020.1:p.His232Gln
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+290C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.432C>A
  hgvsp: ENSP00000440464.1:p.His144Gln
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.432C>A
  hgvsp: ENSP00000349861.3:p.His144Gln
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.435C>A
  hgvsp: ENSP00000375983.1:p.His145Gln
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*577C>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.522C>A
  hgvsp: ENSP00000340171.4:p.His174Gln
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*572C>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His232Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-38230696-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230696
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230696
    reference: chr 19
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+289A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.695A>G
  hgvsp: ENSP00000465020.1:p.His232Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.431A>G
  hgvsp: ENSP00000440464.1:p.His144Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.431A>G
  hgvsp: ENSP00000349861.3:p.His144Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.434A>G
  hgvsp: ENSP00000375983.1:p.His145Arg
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*576A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*571A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.521A>G
  hgvsp: ENSP00000340171.4:p.His174Arg
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20000
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6688
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His232Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

19-38230699-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230699
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230699
    reference: chr 19
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*568C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.518C>T
  hgvsp: ENSP00000340171.4:p.Ser173Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*573C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+286C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.431C>T
  hgvsp: ENSP00000375983.1:p.Ser144Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.428C>T
  hgvsp: ENSP00000440464.1:p.Ser143Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.692C>T
  hgvsp: ENSP00000465020.1:p.Ser231Leu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.428C>T
  hgvsp: ENSP00000349861.3:p.Ser143Leu
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6686
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser231Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

19-38230701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230701
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230701
    reference: chr 19
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.426C>T
  hgvsp: ENST00000357309.3:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.426C>T
  hgvsp: ENST00000536220.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+284C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.516C>T
  hgvsp: ENST00000339503.4:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*571C>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.690C>T
  hgvsp: ENST00000590414.2:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.429C>T
  hgvsp: ENST00000392138.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20000
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23475
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala230Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-38230706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230706
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230706
    reference: chr 19
allele count: 7
allele frequency: 5.768058142026072e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*561T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.421T>C
  hgvsp: ENSP00000349861.3:p.Tyr141His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.424T>C
  hgvsp: ENSP00000375983.1:p.Tyr142His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.685T>C
  hgvsp: ENSP00000465020.1:p.Tyr229His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.511T>C
  hgvsp: ENSP00000340171.4:p.Tyr171His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+279T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*566T>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.421T>C
  hgvsp: ENSP00000440464.1:p.Tyr141His
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr229His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-38230711-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230711
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230711
    reference: chr 19
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.506T>G
  hgvsp: ENSP00000340171.4:p.Phe169Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.419T>G
  hgvsp: ENSP00000375983.1:p.Phe140Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.416T>G
  hgvsp: ENSP00000440464.1:p.Phe139Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*561T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.680T>G
  hgvsp: ENSP00000465020.1:p.Phe227Cys
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*556T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+274T>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.416T>G
  hgvsp: ENSP00000349861.3:p.Phe139Cys
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe227Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

19-38230720-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230720
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230720
    reference: chr 19
allele count: 19117
allele frequency: 1.575049022031078e-1
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.410G>C
  hgvsp: ENSP00000375983.1:p.Gly137Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.671G>C
  hgvsp: ENSP00000465020.1:p.Gly224Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*552G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.407G>C
  hgvsp: ENSP00000349861.3:p.Gly136Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+265G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.497G>C
  hgvsp: ENSP00000340171.4:p.Gly166Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.407G>C
  hgvsp: ENSP00000440464.1:p.Gly136Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*547G>C
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16304
  bin: 2.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.75e1
  variant carriers: 613
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 8.25e1
  variant carriers: 743
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 328
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.25e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.75e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.75e1
  variant carriers: 324
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 9.25e1
  variant carriers: 1000
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 419
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 9.75e1
  variant carriers: 11013
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.75e1
  variant carriers: 882
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 3.25e1
  variant carriers: 186
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 22180
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly224Ala
num of homozygotes: 1737
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

19-38230720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230720
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230720
    reference: chr 19
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.407G>A
  hgvsp: ENSP00000440464.1:p.Gly136Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.497G>A
  hgvsp: ENSP00000340171.4:p.Gly166Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*552G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+265G>A
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.410G>A
  hgvsp: ENSP00000375983.1:p.Gly137Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.407G>A
  hgvsp: ENSP00000349861.3:p.Gly136Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.671G>A
  hgvsp: ENSP00000465020.1:p.Gly224Glu
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*547G>A
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly224Glu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/19-38230725-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230725
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230725
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.666G>T
  hgvsp: ENSP00000465020.1:p.Gln222His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.402G>T
  hgvsp: ENSP00000349861.3:p.Gln134His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.405G>T
  hgvsp: ENSP00000375983.1:p.Gln135His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+260G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.402G>T
  hgvsp: ENSP00000440464.1:p.Gln134His
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*547G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*542G>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.492G>T
  hgvsp: ENSP00000340171.4:p.Gln164His
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3954
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln222His
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: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

19-38230738-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230738
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230738
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*534A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.479A>C
  hgvsp: ENSP00000340171.4:p.Tyr160Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*529A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.389A>C
  hgvsp: ENSP00000349861.3:p.Tyr130Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.653A>C
  hgvsp: ENSP00000465020.1:p.Tyr218Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+247A>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.389A>C
  hgvsp: ENSP00000440464.1:p.Tyr130Ser
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.392A>C
  hgvsp: ENSP00000375983.1:p.Tyr131Ser
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7921
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30383
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr218Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

19-38230742-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230742
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230742
    reference: chr 19
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.649A>G
  hgvsp: ENSP00000465020.1:p.Thr217Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.475A>G
  hgvsp: ENSP00000340171.4:p.Thr159Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*525A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.385A>G
  hgvsp: ENSP00000349861.3:p.Thr129Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+243A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*530A>G
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.388A>G
  hgvsp: ENSP00000375983.1:p.Thr130Ala
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.385A>G
  hgvsp: ENSP00000440464.1:p.Thr129Ala
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr217Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

19-38230743-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230743
    reference: chr 19
allele count: 13
allele frequency: 1.071122536418166e-4
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+242A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.474A>T
  hgvsp: ENSP00000340171.4:p.Lys158Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.648A>T
  hgvsp: ENSP00000465020.1:p.Lys216Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.384A>T
  hgvsp: ENSP00000440464.1:p.Lys128Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.384A>T
  hgvsp: ENSP00000349861.3:p.Lys128Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.387A>T
  hgvsp: ENSP00000375983.1:p.Lys129Asn
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*524A>T
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*529A>T
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys216Asn
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

19-38230746-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38230746
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38230746
    reference: chr 19
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000467929
  ensembl transcript: ENST00000589632
  gene symbol: ZNF573
  hgvsc: ENST00000589632.1:c.*526G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465148
  ensembl transcript: ENST00000586155
  gene symbol: ZNF573
  hgvsc: ENST00000586155.1:c.*521G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000189144
  ensembl transcript: ENST00000590674
  gene symbol: ZNF573
  hgvsc: ENST00000590674.1:n.55+239G>C
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000349861
  ensembl transcript: ENST00000357309
  gene symbol: ZNF573
  hgvsc: ENST00000357309.3:c.381G>C
  hgvsp: ENSP00000349861.3:p.Glu127Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000340171
  ensembl transcript: ENST00000339503
  gene symbol: ZNF573
  hgvsc: ENST00000339503.4:c.471G>C
  hgvsp: ENSP00000340171.4:p.Glu157Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000440464
  ensembl transcript: ENST00000536220
  gene symbol: ZNF573
  hgvsc: ENST00000536220.1:c.381G>C
  hgvsp: ENSP00000440464.1:p.Glu127Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000465020
  ensembl transcript: ENST00000590414
  gene symbol: ZNF573
  hgvsc: ENST00000590414.2:c.645G>C
  hgvsp: ENSP00000465020.1:p.Glu215Asp
  variant of: http://identifiers.org/hgnc/26420
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000189144
  ensembl protein: ENSP00000375983
  ensembl transcript: ENST00000392138
  gene symbol: ZNF573
  hgvsc: ENST00000392138.1:c.384G>C
  hgvsp: ENSP00000375983.1:p.Glu128Asp
  variant of: http://identifiers.org/hgnc/26420
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu215Asp
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1014
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

DP
type: SiteQuality
SIO_000300: 2.650604e6

FS
type: SiteQuality
SIO_000300: 1.962e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20680
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22772
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 11566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

MQ
type: SiteQuality
SIO_000300: 5.828e1

QD
type: SiteQuality
SIO_000300: 1.007e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.914e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.323e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.650388e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.899e0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6605
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22642
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20682
bin: 9.75e1
variant carriers: 2

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.947798987144527e-4
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 4.063e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

DP
type: SiteQuality
SIO_000300: 2.649172e6

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20682
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 4.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.537e1

DP
type: SiteQuality
SIO_000300: 2.649172e6

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

GenotypeQuality
all individuals: 22701
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20685
bin: 9.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 6609
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 7
allele frequency: 4.245511887433285e-4
allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e0

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

FS
type: SiteQuality
SIO_000300: 1.691e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

DP
type: SiteQuality
SIO_000300: 2.648577e6

MQRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

GenotypeQuality
all individuals: 2174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6605
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20679
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.095e0

VQSLOD
type: SiteQuality
SIO_000300: -8.967000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.019e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.005e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 7.125e0

DP
type: SiteQuality
SIO_000300: 2.648046e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20678
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2308
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 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: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.647431e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

QD
type: SiteQuality
SIO_000300: 1.443e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20676
bin: 9.75e1
variant carriers: 3

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004897983713453e-5
allele num: 66558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.744689144416293e-5
allele num: 10262
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.85e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

FS
type: SiteQuality
SIO_000300: 3.202e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 2.646529e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 28

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.606961435570651e-4
allele num: 66538
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 2.646851e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.477e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: -9.595e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

FS
type: SiteQuality
SIO_000300: 2.178e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 2.64196e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -3.93e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1015
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503985561738607e-5
allele num: 66490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
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: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.215e0

FS
type: SiteQuality
SIO_000300: 3.177e0

VQSLOD
type: SiteQuality
SIO_000300: -1.914e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

DP
type: SiteQuality
SIO_000300: 2.639359e6

QD
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
all individuals: 282
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21392
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504936190705514e-5
allele num: 66448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 3.198e0

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.701e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 2.633272e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 795
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variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66414
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: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.481e1

MQ
type: SiteQuality
SIO_000300: 5.998e1

FS
type: SiteQuality
SIO_000300: 6.416e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 2.622089e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.963e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.797e0

GenotypeQuality
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bin: 2.5e0
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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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 803
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.447381302006853e-4
allele num: 16344
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.795e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 2.464e0

QD
type: SiteQuality
SIO_000300: 1.305e1

DP
type: SiteQuality
SIO_000300: 2.621316e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
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: 904
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.837e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.368e1

FS
type: SiteQuality
SIO_000300: 1.2295e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.620894e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2162
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GenotypeQuality
all individuals: 456
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
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: 13
allele frequency: 1.503585473051122e-3
allele num: 8646
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.973e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.591e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.38e0

VQSLOD
type: SiteQuality
SIO_000300: -6.036e0

DP
type: SiteQuality
SIO_000300: 2.620769e6

MQ
type: SiteQuality
SIO_000300: 5.061e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 5.38e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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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bin: 9.75e1
variant carriers: 13

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.75e1
variant carriers: 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: 13
allele frequency: 1.503585473051122e-3
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.202999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.008e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.287e0

DP
type: SiteQuality
SIO_000300: 2.62082e6

QD
type: SiteQuality
SIO_000300: 1.571e1

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: 13

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
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bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.503933364183248e-3
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.176e0

QD
type: SiteQuality
SIO_000300: 1.575e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.205e0

DP
type: SiteQuality
SIO_000300: 2.620553e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.998e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

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

East Asian
type: Population
allele count: 13
allele frequency: 1.504281416338811e-3
allele num: 8642
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: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

FS
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 1.512e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e0

MQ
type: SiteQuality
SIO_000300: 5.08e1

DP
type: SiteQuality
SIO_000300: 2.620843e6

MQRankSum
type: SiteQuality
SIO_000300: -8.351000000000001e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.703e0

VQSLOD
type: SiteQuality
SIO_000300: -5.616e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 3.349e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.621694e6

QD
type: SiteQuality
SIO_000300: 1.574e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.023e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 3.122e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

QD
type: SiteQuality
SIO_000300: 1.104e1

DP
type: SiteQuality
SIO_000300: 2.622031e6

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: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 2.631232e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.03e-1

QD
type: SiteQuality
SIO_000300: 1.555e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.801e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.945525291828794e-4
allele num: 10280
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10290
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

Latino
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allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.7e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

QD
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.905e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

GenotypeQuality
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variant carriers: 1

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.638995e6

FS
type: SiteQuality
SIO_000300: 4.9226e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 1.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.228e1

MQ
type: SiteQuality
SIO_000300: 5.914e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.203e0

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: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
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: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.100000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.301e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.639166e6

QD
type: SiteQuality
SIO_000300: 1.166e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.640525e6

MQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.659e0

FS
type: SiteQuality
SIO_000300: 1.1052e1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

QD
type: SiteQuality
SIO_000300: 1.762e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

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
all individuals: 1591
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.820388349514563e-4
allele num: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 10344
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.437e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

DP
type: SiteQuality
SIO_000300: 2.642169e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.93e-1

FS
type: SiteQuality
SIO_000300: 2.033e0

DP
type: SiteQuality
SIO_000300: 2.643812e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.005e0

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: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.101e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.292e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

DP
type: SiteQuality
SIO_000300: 2.643816e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

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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variant carriers: 78

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

South Asian
type: Population
allele count: 3
allele frequency: 1.819505094614265e-4
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
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: 72
allele frequency: 1.080302484695715e-3
allele num: 66648
num of homozygotes: 1

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 2.64816e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
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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: 13
allele frequency: 1.95078031212485e-4
allele num: 66640
num of homozygotes: 0

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

Other
type: Population
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allele num: 908
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MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 2.432e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.421e1

DP
type: SiteQuality
SIO_000300: 2.64361e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

GenotypeQuality
all individuals: 6514
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 7.25e1
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
all individuals: 20608
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.882e0

DP
type: SiteQuality
SIO_000300: 2.642965e6

FS
type: SiteQuality
SIO_000300: 5.977e0

VQSLOD
type: SiteQuality
SIO_000300: -5.57e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.431e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

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

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

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

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: 16486
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.584e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

FS
type: SiteQuality
SIO_000300: 5.073e0

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

DP
type: SiteQuality
SIO_000300: 2.642853e6

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 35
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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
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 6521
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variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.81e0

QD
type: SiteQuality
SIO_000300: 1.591e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

FS
type: SiteQuality
SIO_000300: 4.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

DP
type: SiteQuality
SIO_000300: 2.642906e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2266
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 139
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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: 20611
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variant carriers: 1

GenotypeQuality
all individuals: 1591
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 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: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.143e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 2.63833e6

VQSLOD
type: SiteQuality
SIO_000300: -3.188e0

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.581e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 20609
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2951
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variant carriers: 0

GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 1591
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variant carriers: 0

GenotypeQuality
all individuals: 22552
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 7.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.262e1

DP
type: SiteQuality
SIO_000300: 2.637949e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.14e-2

FS
type: SiteQuality
SIO_000300: 8.484e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

GenotypeQuality
all individuals: 1589
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 167
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GenotypeQuality
all individuals: 1022
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GenotypeQuality
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GenotypeQuality
all individuals: 20610
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2954
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001380635092142e-5
allele num: 66636
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

FS
type: SiteQuality
SIO_000300: 5.958e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.65e-1

DP
type: SiteQuality
SIO_000300: 2.635966e6

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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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variant carriers: 1240

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 22022
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 246
allele frequency: 1.497625715329356e-2
allele num: 16426
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 80
allele frequency: 1.209555488358029e-2
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 59
allele frequency: 5.09675190048376e-3
allele num: 11576
num of homozygotes: 1

African
type: Population
allele count: 13
allele frequency: 1.249759661603538e-3
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 848
allele frequency: 1.272699984991746e-2
allele num: 66630
num of homozygotes: 7

Other
type: Population
allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.696585e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.302e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.27e0

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

GenotypeQuality
all individuals: 22536
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 336
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 1601
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 223
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GenotypeQuality
all individuals: 20031
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1016
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variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 7.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

East Asian
type: Population
allele count: 18
allele frequency: 2.080443828016643e-3
allele num: 8652
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.647e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.294e1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.61414e6

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
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variant carriers: 0

GenotypeQuality
all individuals: 22114
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 393
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GenotypeQuality
all individuals: 6493
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GenotypeQuality
all individuals: 2998
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GenotypeQuality
all individuals: 290
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 207
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GenotypeQuality
all individuals: 1018
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e0

VQSLOD
type: SiteQuality
SIO_000300: -2.968e0

QD
type: SiteQuality
SIO_000300: 5.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 1.655e0

DP
type: SiteQuality
SIO_000300: 2.608959e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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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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bin: 4.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.123e0

QD
type: SiteQuality
SIO_000300: 1.205e1

DP
type: SiteQuality
SIO_000300: 2.609374e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 6.023e1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

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

GenotypeQuality
all individuals: 248
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 1.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

DP
type: SiteQuality
SIO_000300: 2.609374e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

QD
type: SiteQuality
SIO_000300: 1.205e1

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 6.023e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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: 163
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.221150323604836e-4
allele num: 16378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.125e0

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

DP
type: SiteQuality
SIO_000300: 2.60924e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.609845e6

FS
type: SiteQuality
SIO_000300: 1.787e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.533e0

QD
type: SiteQuality
SIO_000300: 1.313e1

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

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: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.728e1

QD
type: SiteQuality
SIO_000300: 1.585e1

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: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.873e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.23e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

MQRankSum
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VQSLOD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

Other
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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FS
type: SiteQuality
SIO_000300: 1.4005e1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

DP
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22976
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0804e1

MQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e0

DP
type: SiteQuality
SIO_000300: 2.618067e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.022e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 22928
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3061
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1606
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20021
bin: 9.75e1
variant carriers: 37

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.350540216086435e-4
allele num: 66640
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: 25
allele frequency: 2.403846153846154e-3
allele num: 10400
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 2.621105e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 2.618633e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

QD
type: SiteQuality
SIO_000300: 1.482e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

FS
type: SiteQuality
SIO_000300: 3.399e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 23171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20007
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.209e1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.088e0

DP
type: SiteQuality
SIO_000300: 2.619659e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.783e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2230
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23334
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6667
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20009
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2399
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
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: 16490
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

QD
type: SiteQuality
SIO_000300: 1.184e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e0

DP
type: SiteQuality
SIO_000300: 2.621424e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

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

GenotypeQuality
all individuals: 20012
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6677
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2398
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2228
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

FS
type: SiteQuality
SIO_000300: 5.357e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

DP
type: SiteQuality
SIO_000300: 2.622047e6

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.488e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 73
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
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GenotypeQuality
all individuals: 2400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.427e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.582e0

FS
type: SiteQuality
SIO_000300: 1.0155e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 2.622455e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1608
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
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variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6685
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.423e0

QD
type: SiteQuality
SIO_000300: 1.409e1

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 2.622924e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 5.018e0

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 6688
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20012
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
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variant carriers: 0

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

GenotypeQuality
all individuals: 2404
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GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 11
allele frequency: 1.057488944433763e-3
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 7
allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.623826e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.39e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.322e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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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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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
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
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: 10402
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.75e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

DP
type: SiteQuality
SIO_000300: 2.622326e6

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.025e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.882e1

FS
type: SiteQuality
SIO_000300: 4.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.328e0

VQSLOD
type: SiteQuality
SIO_000300: -2.395e0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

DP
type: SiteQuality
SIO_000300: 2.62251e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

QD
type: SiteQuality
SIO_000300: 2.764e1

FS
type: SiteQuality
SIO_000300: 2.1122e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

QD
type: SiteQuality
SIO_000300: 1.622e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.355e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 2.622568e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049475262368816e-4
allele num: 66700
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.543e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.59e0

DP
type: SiteQuality
SIO_000300: 2.623066e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-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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GenotypeQuality
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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: 19995
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.216e1

FS
type: SiteQuality
SIO_000300: 1.9868e1

DP
type: SiteQuality
SIO_000300: 2.622628e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: -3.302e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 22874
bin: 9.75e1
variant carriers: 17342

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10
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GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 949
allele frequency: 8.196579720158922e-2
allele num: 11578
num of homozygotes: 47

African
type: Population
allele count: 544
allele frequency: 5.228758169934641e-2
allele num: 10404
num of homozygotes: 13

South Asian
type: Population
allele count: 1553
allele frequency: 9.408699866715134e-2
allele num: 16506
num of homozygotes: 89

East Asian
type: Population
allele count: 634
allele frequency: 7.327785483125289e-2
allele num: 8652
num of homozygotes: 21

European (Non-Finnish)
type: Population
allele count: 13769
allele frequency: 2.063946516368869e-1
allele num: 66712
num of homozygotes: 1382

European (Finnish)
type: Population
allele count: 1493
allele frequency: 2.257332930148171e-1
allele num: 6614
num of homozygotes: 171

Other
type: Population
allele count: 175
allele frequency: 1.927312775330396e-1
allele num: 908
num of homozygotes: 14

VQSLOD
type: SiteQuality
SIO_000300: 6.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.595e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.73e-1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.347201e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

QD
type: SiteQuality
SIO_000300: 1.611e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.595e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.347201e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 2.008872e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 3942
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GenotypeQuality
all individuals: 2850
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 9012
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.008033e6

QD
type: SiteQuality
SIO_000300: 1.447e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

MQ
type: SiteQuality
SIO_000300: 5.989e1

FS
type: SiteQuality
SIO_000300: 1.926e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.140000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30339
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1880
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3943
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

DP
type: SiteQuality
SIO_000300: 2.007674e6

MQRankSum
type: SiteQuality
SIO_000300: -8.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 3.838e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

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

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

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

GenotypeQuality
all individuals: 3944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7920
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2848
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648977633867002e-4
allele num: 66708
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: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

DP
type: SiteQuality
SIO_000300: 2.007831e6

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.534e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3