8-82615239-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615239
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615239
    reference: chr 8
allele count: 1
allele frequency: 1.27219988804641e-5
allele num: 78604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.280A>G
  hgvsp: ENSP00000429527.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.280A>G
  hgvsp: ENSP00000428278.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*145A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1152A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.280A>G
  hgvsp: ENSP00000429999.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.601A>G
  hgvsp: ENSP00000220669.5:p.Arg201Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.280A>G
  hgvsp: ENSP00000428101.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.280A>G
  hgvsp: ENSP00000430214.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.580A>G
  hgvsp: ENSP00000430736.1:p.Arg194Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.601A>G
  hgvsp: ENSP00000429167.1:p.Arg201Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.280A>G
  hgvsp: ENSP00000428139.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*21A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.125A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*145A>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17138
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg201Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

8-82615242-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615242
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615242
    reference: chr 8
allele count: 13
allele frequency: 1.619735858460005e-4
allele num: 80260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.122G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*142G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.598G>C
  hgvsp: ENSP00000429167.1:p.Ala200Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.277G>C
  hgvsp: ENSP00000430214.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.277G>C
  hgvsp: ENSP00000429999.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.277G>C
  hgvsp: ENSP00000428101.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.277G>C
  hgvsp: ENSP00000428139.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.598G>C
  hgvsp: ENSP00000220669.5:p.Ala200Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.577G>C
  hgvsp: ENSP00000430736.1:p.Ala193Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1149G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.277G>C
  hgvsp: ENSP00000428278.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.277G>C
  hgvsp: ENSP00000429527.1:p.Ala93Pro
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*142G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*18G>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala200Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

8-82615242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615242
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615242
    reference: chr 8
allele count: 1
allele frequency: 1.24595066035385e-5
allele num: 80260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.577G>A
  hgvsp: ENSP00000430736.1:p.Ala193Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.277G>A
  hgvsp: ENSP00000428278.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.277G>A
  hgvsp: ENSP00000429999.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.277G>A
  hgvsp: ENSP00000428139.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.598G>A
  hgvsp: ENSP00000220669.5:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.122G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1149G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*142G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.277G>A
  hgvsp: ENSP00000428101.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*142G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.598G>A
  hgvsp: ENSP00000429167.1:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.277G>A
  hgvsp: ENSP00000429527.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.277G>A
  hgvsp: ENSP00000430214.1:p.Ala93Thr
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala200Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-82615251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615251
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615251
    reference: chr 8
allele count: 1
allele frequency: 1.159635410626899e-5
allele num: 86234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.268G>T
  hgvsp: ENSP00000428139.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.268G>T
  hgvsp: ENSP00000428278.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.268G>T
  hgvsp: ENSP00000429527.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*133G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.589G>T
  hgvsp: ENSP00000429167.1:p.Ala197Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.268G>T
  hgvsp: ENSP00000430214.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*133G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.268G>T
  hgvsp: ENSP00000428101.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1140G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.568G>T
  hgvsp: ENSP00000430736.1:p.Ala190Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.589G>T
  hgvsp: ENSP00000220669.5:p.Ala197Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*9G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.268G>T
  hgvsp: ENSP00000429999.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.113G>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala197Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-82615251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615251
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615251
    reference: chr 8
allele count: 15
allele frequency: 1.739453115940348e-4
allele num: 86234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.268G>A
  hgvsp: ENSP00000429527.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.268G>A
  hgvsp: ENSP00000429999.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.268G>A
  hgvsp: ENSP00000430214.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.113G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1140G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.268G>A
  hgvsp: ENSP00000428101.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.589G>A
  hgvsp: ENSP00000220669.5:p.Ala197Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.268G>A
  hgvsp: ENSP00000428139.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.589G>A
  hgvsp: ENSP00000429167.1:p.Ala197Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.268G>A
  hgvsp: ENSP00000428278.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.568G>A
  hgvsp: ENSP00000430736.1:p.Ala190Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16263
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22494
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala197Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-82615252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615252
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615252
    reference: chr 8
allele count: 17
allele frequency: 1.942501942501943e-4
allele num: 87516
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.588C>T
  hgvsp: ENST00000220669.5:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.267C>T
  hgvsp: ENST00000520635.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.112C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.267C>T
  hgvsp: ENST00000520604.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.267C>T
  hgvsp: ENST00000517588.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.267C>T
  hgvsp: ENST00000521287.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.588C>T
  hgvsp: ENST00000519523.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.267C>T
  hgvsp: ENST00000521895.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1139C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.567C>T
  hgvsp: ENST00000523096.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.267C>T
  hgvsp: ENST00000522520.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*132C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*132C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*8C>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23250
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15779
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala196Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

8-82615258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615258
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615258
    reference: chr 8
allele count: 130
allele frequency: 1.402978631556227e-3
allele num: 92660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1133C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.261C>T
  hgvsp: ENST00000521287.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.106C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.261C>T
  hgvsp: ENST00000520635.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.561C>T
  hgvsp: ENST00000523096.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.582C>T
  hgvsp: ENST00000220669.5:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.261C>T
  hgvsp: ENST00000521895.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.582C>T
  hgvsp: ENST00000519523.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.261C>T
  hgvsp: ENST00000517588.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.261C>T
  hgvsp: ENST00000522520.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.261C>T
  hgvsp: ENST00000520604.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26578
  bin: 2.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 9029
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13691
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Asp194Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-82615260-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615260
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615260
    reference: chr 8
allele count: 3
allele frequency: 3.196794680533652e-5
allele num: 93844
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.259G>T
  hgvsp: ENSP00000430214.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.559G>T
  hgvsp: ENSP00000430736.1:p.Asp187Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*124G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.580G>T
  hgvsp: ENSP00000429167.1:p.Asp194Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*124G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.259G>T
  hgvsp: ENSP00000429527.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.186G>T
  hgvsp: ENSP00000430499.1:p.Ter62TyrextTer6
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.259G>T
  hgvsp: ENSP00000429999.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.580G>T
  hgvsp: ENSP00000220669.5:p.Asp194Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.259G>T
  hgvsp: ENSP00000428278.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.104G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.259G>T
  hgvsp: ENSP00000428101.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.259G>T
  hgvsp: ENSP00000428139.1:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter62TyrextTer6
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS

8-82615261-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615261
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615261
    reference: chr 8
allele count: 21
allele frequency: 2.221328989401087e-4
allele num: 94538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.258A>G
  hgvsp: ENSP00000429999.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.558A>G
  hgvsp: ENSP00000430736.1:p.Ile186Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.579A>G
  hgvsp: ENSP00000429167.1:p.Ile193Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.258A>G
  hgvsp: ENSP00000428101.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*123A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.185A>G
  hgvsp: ENSP00000430499.1:p.Ter62TrpextTer6
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1130A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.103A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*123A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.258A>G
  hgvsp: ENSP00000430214.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.258A>G
  hgvsp: ENSP00000428278.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.579A>G
  hgvsp: ENSP00000220669.5:p.Ile193Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.258A>G
  hgvsp: ENSP00000429527.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.258A>G
  hgvsp: ENSP00000428139.1:p.Ile86Met
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12886
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ter62TrpextTer6
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

8-82615263-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615263
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615263
    reference: chr 8
allele count: 1
allele frequency: 1.046222092025695e-5
allele num: 95582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.256A>G
  hgvsp: ENSP00000428278.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*121A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.101A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.256A>G
  hgvsp: ENSP00000429527.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1128A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.256A>G
  hgvsp: ENSP00000430214.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.256A>G
  hgvsp: ENSP00000429999.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.577A>G
  hgvsp: ENSP00000220669.5:p.Ile193Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.577A>G
  hgvsp: ENSP00000429167.1:p.Ile193Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.256A>G
  hgvsp: ENSP00000428101.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.556A>G
  hgvsp: ENSP00000430736.1:p.Ile186Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.183A>G
  hgvsp: ENST00000522032.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.256A>G
  hgvsp: ENSP00000428139.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*121A>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28791
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile193Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

8-82615274-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615274
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615274
    reference: chr 8
allele count: 1
allele frequency: 9.785118791342127e-6
allele num: 102196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.245T>A
  hgvsp: ENSP00000428139.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.545T>A
  hgvsp: ENSP00000430736.1:p.Ile182Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*110T>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.245T>A
  hgvsp: ENSP00000430214.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.245T>A
  hgvsp: ENSP00000429527.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1117T>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.245T>A
  hgvsp: ENSP00000428278.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.90T>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.172T>A
  hgvsp: ENSP00000430499.1:p.Leu58Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.566T>A
  hgvsp: ENSP00000220669.5:p.Ile189Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.245T>A
  hgvsp: ENSP00000428101.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.566T>A
  hgvsp: ENSP00000429167.1:p.Ile189Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.245T>A
  hgvsp: ENSP00000429999.1:p.Ile82Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*110T>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile189Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-82615274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615274
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615274
    reference: chr 8
allele count: 6
allele frequency: 5.871071274805276e-5
allele num: 102196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.245T>C
  hgvsp: ENSP00000429999.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.90T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.545T>C
  hgvsp: ENSP00000430736.1:p.Ile182Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.245T>C
  hgvsp: ENSP00000428139.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.566T>C
  hgvsp: ENSP00000429167.1:p.Ile189Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.245T>C
  hgvsp: ENSP00000428101.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.172T>C
  hgvsp: ENST00000522032.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.245T>C
  hgvsp: ENSP00000429527.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.245T>C
  hgvsp: ENSP00000430214.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.566T>C
  hgvsp: ENSP00000220669.5:p.Ile189Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.245T>C
  hgvsp: ENSP00000428278.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1117T>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33285
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile189Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

8-82615276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615276
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615276
    reference: chr 8
allele count: 1
allele frequency: 9.697816051825129e-6
allele num: 103116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.243C>T
  hgvsp: ENST00000520635.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.243C>T
  hgvsp: ENST00000521895.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*108C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.170C>T
  hgvsp: ENSP00000430499.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.564C>T
  hgvsp: ENST00000519523.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.564C>T
  hgvsp: ENST00000220669.5:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.243C>T
  hgvsp: ENST00000517588.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*108C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.243C>T
  hgvsp: ENST00000521287.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.88C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.243C>T
  hgvsp: ENST00000520604.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1115C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.243C>T
  hgvsp: ENST00000522520.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.543C>T
  hgvsp: ENST00000523096.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala57Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

8-82615277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615277
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615277
    reference: chr 8
allele count: 2
allele frequency: 1.929533438814495e-5
allele num: 103652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.242G>A
  hgvsp: ENSP00000429527.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.242G>A
  hgvsp: ENSP00000428101.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.542G>A
  hgvsp: ENSP00000430736.1:p.Ser181Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.242G>A
  hgvsp: ENSP00000428278.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1114G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.87G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.242G>A
  hgvsp: ENSP00000429999.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.242G>A
  hgvsp: ENSP00000430214.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.563G>A
  hgvsp: ENSP00000429167.1:p.Ser188Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.169G>A
  hgvsp: ENSP00000430499.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.563G>A
  hgvsp: ENSP00000220669.5:p.Ser188Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.242G>A
  hgvsp: ENSP00000428139.1:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34322
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser188Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-82615283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615283
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615283
    reference: chr 8
allele count: 2
allele frequency: 1.871502629461194e-5
allele num: 106866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*101G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.236G>A
  hgvsp: ENSP00000429999.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.236G>A
  hgvsp: ENSP00000430214.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.163G>A
  hgvsp: ENSP00000430499.1:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.236G>A
  hgvsp: ENSP00000428139.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.557G>A
  hgvsp: ENSP00000220669.5:p.Arg186Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*101G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.236G>A
  hgvsp: ENSP00000429527.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.557G>A
  hgvsp: ENSP00000429167.1:p.Arg186Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.236G>A
  hgvsp: ENSP00000428101.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.536G>A
  hgvsp: ENSP00000430736.1:p.Arg179Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.81G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1108G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.236G>A
  hgvsp: ENSP00000428278.1:p.Arg79Gln
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg186Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

8-82615284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615284
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615284
    reference: chr 8
allele count: 1
allele frequency: 9.300076260625336e-6
allele num: 107526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.235C>T
  hgvsp: ENSP00000428139.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.235C>T
  hgvsp: ENSP00000430214.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.535C>T
  hgvsp: ENSP00000430736.1:p.Arg179Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.235C>T
  hgvsp: ENSP00000429999.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.162C>T
  hgvsp: ENST00000522032.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.80C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.556C>T
  hgvsp: ENSP00000429167.1:p.Arg186Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*100C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.235C>T
  hgvsp: ENSP00000428101.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.235C>T
  hgvsp: ENSP00000428278.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.235C>T
  hgvsp: ENSP00000429527.1:p.Arg79Ter
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1107C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*100C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.556C>T
  hgvsp: ENSP00000220669.5:p.Arg186Ter
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg186Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-82615289-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615289
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615289
    reference: chr 8
allele count: 4
allele frequency: 3.632401017072285e-5
allele num: 110120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1102G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.157G>A
  hgvsp: ENSP00000430499.1:p.Ala53Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.230G>A
  hgvsp: ENSP00000428278.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.230G>A
  hgvsp: ENSP00000428101.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.230G>A
  hgvsp: ENSP00000429527.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.530G>A
  hgvsp: ENSP00000430736.1:p.Cys177Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.230G>A
  hgvsp: ENSP00000428139.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.230G>A
  hgvsp: ENSP00000430214.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.230G>A
  hgvsp: ENSP00000429999.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*95G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.551G>A
  hgvsp: ENSP00000429167.1:p.Cys184Tyr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*95G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.75G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.551G>A
  hgvsp: ENSP00000220669.5:p.Cys184Tyr
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9224
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys184Tyr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-82615302-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615302
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615302
    reference: chr 8
allele count: 2
allele frequency: 1.777840989901863e-5
allele num: 112496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.62C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.217C>G
  hgvsp: ENSP00000430214.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.217C>G
  hgvsp: ENSP00000428278.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.217C>G
  hgvsp: ENSP00000429527.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*82C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.538C>G
  hgvsp: ENSP00000220669.5:p.Pro180Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.144C>G
  hgvsp: ENSP00000430499.1:p.Asn48Lys
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.217C>G
  hgvsp: ENSP00000429999.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*82C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.217C>G
  hgvsp: ENSP00000428139.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.217C>G
  hgvsp: ENSP00000428101.1:p.Pro73Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.538C>G
  hgvsp: ENSP00000429167.1:p.Pro180Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.517C>G
  hgvsp: ENSP00000430736.1:p.Pro173Ala
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1089C>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro180Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-82615314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615314
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615314
    reference: chr 8
allele count: 1
allele frequency: 8.889046916389624e-6
allele num: 112498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.205G>C
  hgvsp: ENSP00000430214.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.205G>C
  hgvsp: ENSP00000428139.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.526G>C
  hgvsp: ENSP00000429167.1:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.132G>C
  hgvsp: ENSP00000430499.1:p.Lys44Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1077G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*70G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.50G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.505G>C
  hgvsp: ENSP00000430736.1:p.Glu169Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.205G>C
  hgvsp: ENSP00000429527.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.205G>C
  hgvsp: ENSP00000428278.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.205G>C
  hgvsp: ENSP00000428101.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*70G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.205G>C
  hgvsp: ENSP00000429999.1:p.Glu69Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.526G>C
  hgvsp: ENSP00000220669.5:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu176Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-82615319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615319
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615319
    reference: chr 8
allele count: 1
allele frequency: 8.887782853689319e-6
allele num: 112514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.200G>A
  hgvsp: ENSP00000429999.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.200G>A
  hgvsp: ENSP00000430214.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.521G>A
  hgvsp: ENSP00000220669.5:p.Ser174Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.127G>A
  hgvsp: ENSP00000430499.1:p.Ala43Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.521G>A
  hgvsp: ENSP00000429167.1:p.Ser174Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.200G>A
  hgvsp: ENSP00000429527.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.200G>A
  hgvsp: ENSP00000428101.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.200G>A
  hgvsp: ENSP00000428278.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*65G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*65G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.200G>A
  hgvsp: ENSP00000428139.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.500G>A
  hgvsp: ENSP00000430736.1:p.Ser167Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.45G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1072G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser174Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-82615320-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615320
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615320
    reference: chr 8
allele count: 2
allele frequency: 1.783834888242744e-5
allele num: 112118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*64A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.499A>G
  hgvsp: ENSP00000430736.1:p.Ser167Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.199A>G
  hgvsp: ENSP00000428139.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.199A>G
  hgvsp: ENSP00000430214.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*64A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.520A>G
  hgvsp: ENSP00000220669.5:p.Ser174Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.44A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.199A>G
  hgvsp: ENSP00000428101.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.199A>G
  hgvsp: ENSP00000429999.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.520A>G
  hgvsp: ENSP00000429167.1:p.Ser174Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.199A>G
  hgvsp: ENSP00000429527.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1071A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.126A>G
  hgvsp: ENST00000522032.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.199A>G
  hgvsp: ENSP00000428278.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser174Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

8-82615321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615321
    reference: chr 8
allele count: 41
allele frequency: 3.656274523792538e-4
allele num: 112136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.519G>A
  hgvsp: ENST00000519523.1:c.519G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.198G>A
  hgvsp: ENST00000520635.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.198G>A
  hgvsp: ENST00000520604.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.198G>A
  hgvsp: ENST00000517588.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.198G>A
  hgvsp: ENST00000522520.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1070G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.125G>A
  hgvsp: ENSP00000430499.1:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.198G>A
  hgvsp: ENST00000521895.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.498G>A
  hgvsp: ENST00000523096.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.43G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.519G>A
  hgvsp: ENST00000220669.5:c.519G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*63G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*63G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.198G>A
  hgvsp: ENST00000521287.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly42Glu
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-82615325-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615325
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615325
    reference: chr 8
allele count: 1
allele frequency: 8.96426842605375e-6
allele num: 111554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.194A>C
  hgvsp: ENSP00000428101.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.194A>C
  hgvsp: ENSP00000428278.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.515A>C
  hgvsp: ENSP00000429167.1:p.Lys172Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.494A>C
  hgvsp: ENSP00000430736.1:p.Lys165Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-3A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.194A>C
  hgvsp: ENSP00000428139.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*59A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.515A>C
  hgvsp: ENSP00000220669.5:p.Lys172Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.194A>C
  hgvsp: ENSP00000429999.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.194A>C
  hgvsp: ENSP00000429527.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.194A>C
  hgvsp: ENSP00000430214.1:p.Lys65Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*59A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1066A>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys172Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-82615327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615327
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615327
    reference: chr 8
allele count: 1
allele frequency: 8.994423457456377e-6
allele num: 111180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.192T>C
  hgvsp: ENST00000520604.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.192T>C
  hgvsp: ENST00000522520.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.513T>C
  hgvsp: ENST00000519523.1:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-5T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1064T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.192T>C
  hgvsp: ENST00000521287.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.492T>C
  hgvsp: ENST00000523096.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.513T>C
  hgvsp: ENST00000220669.5:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.192T>C
  hgvsp: ENST00000521895.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.37T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.192T>C
  hgvsp: ENST00000517588.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*57T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.192T>C
  hgvsp: ENST00000520635.1:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*57T>C
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.124-5T>C
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: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/8-82615337-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615337
    reference: chr 8
allele count: 21
allele frequency: 1.921739448735312e-4
allele num: 109276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*47T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.182T>G
  hgvsp: ENSP00000429999.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.182T>G
  hgvsp: ENSP00000430214.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.182T>G
  hgvsp: ENSP00000427957.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.503T>G
  hgvsp: ENSP00000429167.1:p.Val168Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.482T>G
  hgvsp: ENSP00000430736.1:p.Val161Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.27T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.503T>G
  hgvsp: ENSP00000220669.5:p.Val168Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1054T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.182T>G
  hgvsp: ENSP00000428101.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.182T>G
  hgvsp: ENSP00000428139.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.182T>G
  hgvsp: ENSP00000429527.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-15T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*47T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.182T>G
  hgvsp: ENSP00000428278.1:p.Val61Gly
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4195
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10271
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36937
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Val168Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-82615350-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615350
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615350
    reference: chr 8
allele count: 1
allele frequency: 9.440196356084207e-6
allele num: 105930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-12A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.169A>T
  hgvsp: ENSP00000428139.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.169A>T
  hgvsp: ENSP00000428278.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.169A>T
  hgvsp: ENSP00000429527.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1041A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.490A>T
  hgvsp: ENSP00000429167.1:p.Ile164Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000519338
  gene symbol: ZFAND1
  hgvsc: ENST00000519338.1:n.14A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.169A>T
  hgvsp: ENSP00000427957.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-28A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*34A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.169A>T
  hgvsp: ENSP00000429999.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.490A>T
  hgvsp: ENSP00000220669.5:p.Ile164Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.169A>T
  hgvsp: ENSP00000430214.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.169A>T
  hgvsp: ENSP00000428101.1:p.Ile57Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*34A>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile164Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-82615363-TAAAAAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615363
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615357
    reference: chr 8
allele count: 2
allele frequency: 1.968348948901661e-5
allele num: 101608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-10_*25-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-10_481-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-31_481-26delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-10_481-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-10_*25-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-10_1032-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-47_124-42delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-10_160-5delCTTTTT
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.481-10_481-5delCTTTTT
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: TAAAAAG
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

8-82615385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615385
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615385
    reference: chr 8
allele count: 1
allele frequency: 1.041384624997397e-5
allele num: 96026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-47G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-63G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

8-82615386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615386
    reference: chr 8
allele count: 1
allele frequency: 1.046265877084685e-5
allele num: 95578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-64G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-48G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-27G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-27G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

8-82615391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615391
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615391
    reference: chr 8
allele count: 1
allele frequency: 1.060647843702934e-5
allele num: 94282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-53G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-69G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-32G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-82615393-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615393
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615393
    reference: chr 8
allele count: 2
allele frequency: 2.185840127653063e-5
allele num: 91498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-55A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-71A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-34A>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13052
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-82615394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615394
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615394
    reference: chr 8
allele count: 46
allele frequency: 5.016576513697435e-4
allele num: 91696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-56T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-72T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-35T>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12987
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18880
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-82615395-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615395
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615395
    reference: chr 8
allele count: 2
allele frequency: 2.184741763523552e-5
allele num: 91544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-57C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-73C>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-36C>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18884
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-82615401-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82615401
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82615401
    reference: chr 8
allele count: 2
allele frequency: 2.204925804246687e-5
allele num: 90706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.481-63T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.481-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*25-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1032-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*25-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.160-42T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.124-79T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.481-42T>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/8-82621022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82621022
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82621022
    reference: chr 8
allele count: 4
allele frequency: 4.14765657403567e-4
allele num: 9644
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.*24+1G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.*24+1G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+5131G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+5131G>T
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*24+1G>T
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-82621064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82621064
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82621064
    reference: chr 8
allele count: 4
allele frequency: 4.026575397624321e-4
allele num: 9934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.481A>G
  hgvsp: ENSP00000428375.1:p.Met161Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.160A>G
  hgvsp: ENSP00000428927.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+5089A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+5089A>G
  variant of: http://identifiers.org/hgnc/25858
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met54Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-82621090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82621090
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82621090
    reference: chr 8
allele count: 3
allele frequency: 3.097253768325418e-4
allele num: 9686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.160-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.481-26G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+5063G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-82621110-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82621110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82621109
    reference: chr 8
allele count: 1
allele frequency: 1.126126126126126e-4
allele num: 8880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.481-47delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.160-47delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+5042delT
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+5042delT
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: TA
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-82626106-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626106
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626106
    reference: chr 8
allele count: 1
allele frequency: 8.278008642241022e-6
allele num: 120802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+47G>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+47G>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

8-82626112-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626112
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626112
    reference: chr 8
allele count: 2
allele frequency: 1.654150263009892e-5
allele num: 120908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+41A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+41A>G
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-82626114-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626114
    reference: chr 8
allele count: 29
allele frequency: 2.397645346914479e-4
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+39A>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

8-82626121-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626121
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626121
    reference: chr 8
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+32A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+32A>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

8-82626146-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626146
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626146
    reference: chr 8
allele count: 4388
allele frequency: 3.618789998020717e-2
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+7C>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 3.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 12124
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 305
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25313
  bin: 2.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 191
genotype quality: GenotypeQuality
hgvs: c.480+7C>T
num of homozygotes: 98
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-82626147-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626147
    reference: chr 8
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.480+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.480+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.159+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.480+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.480+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.123+6T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1031+6T>C
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.480+6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-82626168-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626168
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626168
    reference: chr 8
allele count: 3
allele frequency: 2.473084595980413e-5
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1016T>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.144T>G
  hgvsp: ENSP00000429527.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.144T>G
  hgvsp: ENSP00000428139.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.144T>G
  hgvsp: ENSP00000427811.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.465T>G
  hgvsp: ENSP00000428375.1:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.144T>G
  hgvsp: ENSP00000428927.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.144T>G
  hgvsp: ENSP00000428278.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.465T>G
  hgvsp: ENSP00000430736.1:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.144T>G
  hgvsp: ENSP00000428101.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.144T>G
  hgvsp: ENSP00000430405.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.144T>G
  hgvsp: ENSP00000430214.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.144T>G
  hgvsp: ENSP00000427957.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.144T>G
  hgvsp: ENSP00000429999.1:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.108T>G
  hgvsp: ENSP00000430499.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.465T>G
  hgvsp: ENSP00000429167.1:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.465T>G
  hgvsp: ENSP00000220669.5:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp155Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ

8-82626170-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626170
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626170
    reference: chr 8
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.142G>C
  hgvsp: ENSP00000428101.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.463G>C
  hgvsp: ENSP00000430736.1:p.Asp155His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.142G>C
  hgvsp: ENSP00000430405.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.142G>C
  hgvsp: ENSP00000428278.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.106G>C
  hgvsp: ENSP00000430499.1:p.Asp36His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.463G>C
  hgvsp: ENSP00000428375.1:p.Asp155His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.142G>C
  hgvsp: ENSP00000427811.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.463G>C
  hgvsp: ENSP00000220669.5:p.Asp155His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1014G>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.142G>C
  hgvsp: ENSP00000428139.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.463G>C
  hgvsp: ENSP00000429167.1:p.Asp155His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.142G>C
  hgvsp: ENSP00000429999.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.142G>C
  hgvsp: ENSP00000429527.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.142G>C
  hgvsp: ENSP00000427957.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.142G>C
  hgvsp: ENSP00000428927.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.142G>C
  hgvsp: ENSP00000430214.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp155His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

8-82626170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626170
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626170
    reference: chr 8
allele count: 3
allele frequency: 2.473084595980413e-5
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.142G>A
  hgvsp: ENSP00000428139.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.463G>A
  hgvsp: ENSP00000430736.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.142G>A
  hgvsp: ENSP00000430405.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.142G>A
  hgvsp: ENSP00000428278.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.463G>A
  hgvsp: ENSP00000429167.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.106G>A
  hgvsp: ENSP00000430499.1:p.Asp36Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.142G>A
  hgvsp: ENSP00000427811.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.142G>A
  hgvsp: ENSP00000430214.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.142G>A
  hgvsp: ENSP00000429527.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.142G>A
  hgvsp: ENSP00000429999.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.142G>A
  hgvsp: ENSP00000428927.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.463G>A
  hgvsp: ENSP00000220669.5:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1014G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.142G>A
  hgvsp: ENSP00000427957.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.142G>A
  hgvsp: ENSP00000428101.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.463G>A
  hgvsp: ENSP00000428375.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp155Asn
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

8-82626171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626171
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626171
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.141C>T
  hgvsp: ENST00000521742.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.141C>T
  hgvsp: ENST00000517450.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.462C>T
  hgvsp: ENST00000519523.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.462C>T
  hgvsp: ENST00000519464.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.462C>T
  hgvsp: ENST00000523096.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.462C>T
  hgvsp: ENST00000220669.5:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.141C>T
  hgvsp: ENST00000521895.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.141C>T
  hgvsp: ENST00000523431.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.141C>T
  hgvsp: ENST00000522520.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.141C>T
  hgvsp: ENST00000517588.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.141C>T
  hgvsp: ENST00000520604.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.141C>T
  hgvsp: ENST00000523361.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.105C>T
  hgvsp: ENST00000522032.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1013C>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.141C>T
  hgvsp: ENST00000521287.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.141C>T
  hgvsp: ENST00000520635.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly154Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

8-82626175-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626175
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626175
    reference: chr 8
allele count: 3
allele frequency: 2.473329266080762e-5
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.458A>T
  hgvsp: ENSP00000429167.1:p.Asp153Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.137A>T
  hgvsp: ENSP00000429527.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.137A>T
  hgvsp: ENSP00000429999.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.137A>T
  hgvsp: ENSP00000428139.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.458A>T
  hgvsp: ENSP00000428375.1:p.Asp153Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.137A>T
  hgvsp: ENSP00000430214.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.137A>T
  hgvsp: ENSP00000430405.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.101A>T
  hgvsp: ENSP00000430499.1:p.Asp34Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.137A>T
  hgvsp: ENSP00000428278.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.458A>T
  hgvsp: ENSP00000430736.1:p.Asp153Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.458A>T
  hgvsp: ENSP00000220669.5:p.Asp153Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.137A>T
  hgvsp: ENSP00000427811.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.137A>T
  hgvsp: ENSP00000428101.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1009A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.137A>T
  hgvsp: ENSP00000427957.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.137A>T
  hgvsp: ENSP00000428927.1:p.Asp46Val
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp153Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

8-82626179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626179
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626179
    reference: chr 8
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.133G>A
  hgvsp: ENSP00000428278.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.454G>A
  hgvsp: ENSP00000220669.5:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.133G>A
  hgvsp: ENSP00000429999.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.133G>A
  hgvsp: ENSP00000430214.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.133G>A
  hgvsp: ENSP00000430405.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.454G>A
  hgvsp: ENSP00000430736.1:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.133G>A
  hgvsp: ENSP00000429527.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.133G>A
  hgvsp: ENSP00000427811.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.454G>A
  hgvsp: ENSP00000428375.1:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.133G>A
  hgvsp: ENSP00000427957.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.133G>A
  hgvsp: ENSP00000428927.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.133G>A
  hgvsp: ENSP00000428139.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1005G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.454G>A
  hgvsp: ENSP00000429167.1:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.133G>A
  hgvsp: ENSP00000428101.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.97G>A
  hgvsp: ENSP00000430499.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala152Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-82626183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626183
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626183
    reference: chr 8
allele count: 6
allele frequency: 4.947719101494211e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.129G>A
  hgvsp: ENSP00000429527.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.129G>A
  hgvsp: ENSP00000430405.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.450G>A
  hgvsp: ENSP00000220669.5:p.Met150Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.1001G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.129G>A
  hgvsp: ENSP00000427957.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.129G>A
  hgvsp: ENSP00000428278.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.129G>A
  hgvsp: ENSP00000428927.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.129G>A
  hgvsp: ENSP00000429999.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.129G>A
  hgvsp: ENSP00000428527.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.129G>A
  hgvsp: ENSP00000428139.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.450G>A
  hgvsp: ENSP00000430736.1:p.Met150Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.129G>A
  hgvsp: ENSP00000427811.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.129G>A
  hgvsp: ENSP00000430214.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.129G>A
  hgvsp: ENSP00000428101.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.93G>A
  hgvsp: ENSP00000430499.1:p.Met31Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.450G>A
  hgvsp: ENSP00000429167.1:p.Met150Ile
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.450G>A
  hgvsp: ENSP00000428375.1:p.Met150Ile
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12400
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met150Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-82626189-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626189
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626189
    reference: chr 8
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.444A>T
  hgvsp: ENSP00000430736.1:p.Leu148Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.123A>T
  hgvsp: ENSP00000430214.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.123A>T
  hgvsp: ENSP00000427957.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.123A>T
  hgvsp: ENSP00000427811.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.123A>T
  hgvsp: ENSP00000429527.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.444A>T
  hgvsp: ENSP00000429167.1:p.Leu148Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.123A>T
  hgvsp: ENSP00000428927.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.995A>T
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.123A>T
  hgvsp: ENSP00000428101.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.123A>T
  hgvsp: ENSP00000429999.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.444A>T
  hgvsp: ENSP00000220669.5:p.Leu148Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.123A>T
  hgvsp: ENSP00000430719.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.87A>T
  hgvsp: ENSP00000430499.1:p.Leu29Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.123A>T
  hgvsp: ENSP00000430405.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.123A>T
  hgvsp: ENSP00000428278.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.123A>T
  hgvsp: ENSP00000428527.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.123A>T
  hgvsp: ENSP00000428139.1:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.444A>T
  hgvsp: ENSP00000428375.1:p.Leu148Phe
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu148Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-82626196-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626196
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626196
    reference: chr 8
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.116T>C
  hgvsp: ENSP00000429999.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.116T>C
  hgvsp: ENSP00000428139.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.116T>C
  hgvsp: ENSP00000430405.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.116T>C
  hgvsp: ENSP00000428278.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.116T>C
  hgvsp: ENSP00000430214.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.116T>C
  hgvsp: ENSP00000427811.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.116T>C
  hgvsp: ENSP00000428527.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.80T>C
  hgvsp: ENSP00000430499.1:p.Met27Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.437T>C
  hgvsp: ENSP00000220669.5:p.Met146Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.116T>C
  hgvsp: ENSP00000428101.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.116T>C
  hgvsp: ENSP00000429527.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.988T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.437T>C
  hgvsp: ENSP00000430736.1:p.Met146Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.116T>C
  hgvsp: ENSP00000427957.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.116T>C
  hgvsp: ENSP00000430719.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.116T>C
  hgvsp: ENSP00000428927.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.437T>C
  hgvsp: ENSP00000429167.1:p.Met146Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.437T>C
  hgvsp: ENSP00000428375.1:p.Met146Thr
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27503
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met146Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-82626200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626200
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626200
    reference: chr 8
allele count: 2
allele frequency: 1.650137786505173e-5
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.112T>C
  hgvsp: ENST00000520604.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.112T>C
  hgvsp: ENST00000520635.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.112T>C
  hgvsp: ENST00000521287.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.112T>C
  hgvsp: ENST00000520076.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.112T>C
  hgvsp: ENST00000521895.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.112T>C
  hgvsp: ENST00000517588.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.112T>C
  hgvsp: ENST00000521742.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.433T>C
  hgvsp: ENST00000519464.1:c.433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.433T>C
  hgvsp: ENST00000519523.1:c.433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.112T>C
  hgvsp: ENST00000517450.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.112T>C
  hgvsp: ENST00000523431.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.433T>C
  hgvsp: ENST00000220669.5:c.433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.76T>C
  hgvsp: ENST00000522032.1:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.433T>C
  hgvsp: ENST00000523096.1:c.433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.984T>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.112T>C
  hgvsp: ENST00000523361.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.112T>C
  hgvsp: ENST00000522520.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.112T>C
  hgvsp: ENST00000518419.1:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu145Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

8-82626200-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626200
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626200
    reference: chr 8
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.112T>A
  hgvsp: ENSP00000430405.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.112T>A
  hgvsp: ENSP00000429999.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.433T>A
  hgvsp: ENSP00000429167.1:p.Leu145Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.112T>A
  hgvsp: ENSP00000428527.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.433T>A
  hgvsp: ENSP00000220669.5:p.Leu145Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.112T>A
  hgvsp: ENSP00000428278.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.112T>A
  hgvsp: ENSP00000429527.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.112T>A
  hgvsp: ENSP00000430214.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.112T>A
  hgvsp: ENSP00000430719.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.76T>A
  hgvsp: ENSP00000430499.1:p.Leu26Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.112T>A
  hgvsp: ENSP00000428139.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.112T>A
  hgvsp: ENSP00000428927.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.112T>A
  hgvsp: ENSP00000427811.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.433T>A
  hgvsp: ENSP00000428375.1:p.Leu145Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.433T>A
  hgvsp: ENSP00000430736.1:p.Leu145Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.984T>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.112T>A
  hgvsp: ENSP00000427957.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.112T>A
  hgvsp: ENSP00000428101.1:p.Leu38Met
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu145Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

8-82626201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626201
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626201
    reference: chr 8
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.432A>G
  hgvsp: ENST00000519464.1:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.432A>G
  hgvsp: ENST00000220669.5:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.111A>G
  hgvsp: ENST00000517450.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.111A>G
  hgvsp: ENST00000523431.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.111A>G
  hgvsp: ENST00000517588.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.111A>G
  hgvsp: ENST00000522520.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.75A>G
  hgvsp: ENST00000522032.1:c.75A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.111A>G
  hgvsp: ENST00000521742.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.111A>G
  hgvsp: ENST00000520635.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.432A>G
  hgvsp: ENST00000523096.1:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.111A>G
  hgvsp: ENST00000520076.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.111A>G
  hgvsp: ENST00000523361.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.111A>G
  hgvsp: ENST00000520604.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.432A>G
  hgvsp: ENST00000519523.1:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.111A>G
  hgvsp: ENST00000521287.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.111A>G
  hgvsp: ENST00000518419.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.983A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.111A>G
  hgvsp: ENST00000521895.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-82626203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626203
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626203
    reference: chr 8
allele count: 5
allele frequency: 4.126502046745016e-5
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.109G>A
  hgvsp: ENSP00000428278.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.109G>A
  hgvsp: ENSP00000430719.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.109G>A
  hgvsp: ENSP00000429999.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.430G>A
  hgvsp: ENSP00000430736.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.109G>A
  hgvsp: ENSP00000428927.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.430G>A
  hgvsp: ENSP00000428375.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.73G>A
  hgvsp: ENSP00000430499.1:p.Ala25Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.109G>A
  hgvsp: ENSP00000430405.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.430G>A
  hgvsp: ENSP00000429167.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.109G>A
  hgvsp: ENSP00000427811.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.109G>A
  hgvsp: ENSP00000428139.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.109G>A
  hgvsp: ENSP00000429527.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.981G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.109G>A
  hgvsp: ENSP00000427957.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.109G>A
  hgvsp: ENSP00000430214.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.109G>A
  hgvsp: ENSP00000428101.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.109G>A
  hgvsp: ENSP00000428527.1:p.Ala37Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.430G>A
  hgvsp: ENSP00000220669.5:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/8-82626206-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626206
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626206
    reference: chr 8
allele count: 2
allele frequency: 1.650846058605035e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.106G>T
  hgvsp: ENSP00000430719.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.427G>T
  hgvsp: ENSP00000430736.1:p.Val143Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.106G>T
  hgvsp: ENSP00000430405.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.427G>T
  hgvsp: ENSP00000429167.1:p.Val143Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.106G>T
  hgvsp: ENSP00000428927.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.427G>T
  hgvsp: ENSP00000428375.1:p.Val143Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.106G>T
  hgvsp: ENSP00000428101.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.106G>T
  hgvsp: ENSP00000427811.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.427G>T
  hgvsp: ENSP00000220669.5:p.Val143Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.106G>T
  hgvsp: ENSP00000428527.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.106G>T
  hgvsp: ENSP00000429999.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.106G>T
  hgvsp: ENSP00000429527.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.106G>T
  hgvsp: ENSP00000430214.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.106G>T
  hgvsp: ENSP00000428278.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.106G>T
  hgvsp: ENSP00000428139.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.70G>T
  hgvsp: ENSP00000430499.1:p.Val24Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.106G>T
  hgvsp: ENSP00000427957.1:p.Val36Phe
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.978G>T
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val143Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

8-82626209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626209
    reference: chr 8
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.424A>G
  hgvsp: ENSP00000428375.1:p.Lys142Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.103A>G
  hgvsp: ENSP00000428139.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.975A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.103A>G
  hgvsp: ENSP00000428101.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.67A>G
  hgvsp: ENSP00000430499.1:p.Lys23Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.103A>G
  hgvsp: ENSP00000427811.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.424A>G
  hgvsp: ENSP00000430736.1:p.Lys142Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.103A>G
  hgvsp: ENSP00000428927.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.103A>G
  hgvsp: ENSP00000430405.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.103A>G
  hgvsp: ENSP00000429999.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.103A>G
  hgvsp: ENSP00000430719.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.424A>G
  hgvsp: ENSP00000220669.5:p.Lys142Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.424A>G
  hgvsp: ENSP00000429167.1:p.Lys142Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.103A>G
  hgvsp: ENSP00000427957.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.103A>G
  hgvsp: ENSP00000428527.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.103A>G
  hgvsp: ENSP00000428278.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.103A>G
  hgvsp: ENSP00000430214.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.103A>G
  hgvsp: ENSP00000429527.1:p.Lys35Glu
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys142Glu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

8-82626209-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626209
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626209
    reference: chr 8
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.103A>C
  hgvsp: ENSP00000427957.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.424A>C
  hgvsp: ENSP00000220669.5:p.Lys142Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.424A>C
  hgvsp: ENSP00000430736.1:p.Lys142Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.103A>C
  hgvsp: ENSP00000428101.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.103A>C
  hgvsp: ENSP00000428278.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.103A>C
  hgvsp: ENSP00000428927.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.103A>C
  hgvsp: ENSP00000427811.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.424A>C
  hgvsp: ENSP00000429167.1:p.Lys142Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.103A>C
  hgvsp: ENSP00000429999.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.103A>C
  hgvsp: ENSP00000428139.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.103A>C
  hgvsp: ENSP00000429527.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.103A>C
  hgvsp: ENSP00000430405.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.103A>C
  hgvsp: ENSP00000430719.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.67A>C
  hgvsp: ENSP00000430499.1:p.Lys23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.103A>C
  hgvsp: ENSP00000430214.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.975A>C
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.103A>C
  hgvsp: ENSP00000428527.1:p.Lys35Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.424A>C
  hgvsp: ENSP00000428375.1:p.Lys142Gln
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys142Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-82626212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626212
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626212
    reference: chr 8
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.100G>A
  hgvsp: ENSP00000428278.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.421G>A
  hgvsp: ENSP00000428375.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.100G>A
  hgvsp: ENSP00000428101.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.100G>A
  hgvsp: ENSP00000428927.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.100G>A
  hgvsp: ENSP00000428139.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.64G>A
  hgvsp: ENSP00000430499.1:p.Ala22Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.100G>A
  hgvsp: ENSP00000430214.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.421G>A
  hgvsp: ENSP00000429167.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.100G>A
  hgvsp: ENSP00000427957.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.100G>A
  hgvsp: ENSP00000429999.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.421G>A
  hgvsp: ENSP00000430736.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.100G>A
  hgvsp: ENSP00000429527.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.100G>A
  hgvsp: ENSP00000430719.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.100G>A
  hgvsp: ENSP00000427811.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.100G>A
  hgvsp: ENSP00000430405.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.100G>A
  hgvsp: ENSP00000428527.1:p.Ala34Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.421G>A
  hgvsp: ENSP00000220669.5:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.972G>A
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala141Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-82626226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626226
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626226
    reference: chr 8
allele count: 4
allele frequency: 3.309504898067249e-5
allele num: 120864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.958A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.50A>G
  hgvsp: ENSP00000430499.1:p.Asn17Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.86A>G
  hgvsp: ENSP00000428278.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.86A>G
  hgvsp: ENSP00000427811.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.86A>G
  hgvsp: ENSP00000429999.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.407A>G
  hgvsp: ENSP00000428375.1:p.Asn136Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.86A>G
  hgvsp: ENSP00000428101.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.86A>G
  hgvsp: ENSP00000430719.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.407A>G
  hgvsp: ENSP00000429167.1:p.Asn136Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.407A>G
  hgvsp: ENSP00000430736.1:p.Asn136Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.407A>G
  hgvsp: ENSP00000220669.5:p.Asn136Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.86A>G
  hgvsp: ENSP00000427957.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.86A>G
  hgvsp: ENSP00000428139.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.86A>G
  hgvsp: ENSP00000429527.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.86A>G
  hgvsp: ENSP00000430214.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.86A>G
  hgvsp: ENSP00000430405.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.86A>G
  hgvsp: ENSP00000428527.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.86A>G
  hgvsp: ENSP00000428927.1:p.Asn29Ser
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn136Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

8-82626229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626229
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626229
    reference: chr 8
allele count: 1
allele frequency: 8.278008642241022e-6
allele num: 120802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.83A>G
  hgvsp: ENSP00000428101.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.83A>G
  hgvsp: ENSP00000427811.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.404A>G
  hgvsp: ENSP00000429167.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.47A>G
  hgvsp: ENSP00000430499.1:p.Lys16Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.83A>G
  hgvsp: ENSP00000430214.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.83A>G
  hgvsp: ENSP00000430405.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.83A>G
  hgvsp: ENSP00000429999.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.83A>G
  hgvsp: ENSP00000428278.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.955A>G
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.83A>G
  hgvsp: ENSP00000427957.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.404A>G
  hgvsp: ENSP00000428375.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.404A>G
  hgvsp: ENSP00000430736.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.83A>G
  hgvsp: ENSP00000430719.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.404A>G
  hgvsp: ENSP00000220669.5:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.83A>G
  hgvsp: ENSP00000428527.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.83A>G
  hgvsp: ENSP00000428927.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.83A>G
  hgvsp: ENSP00000428139.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.83A>G
  hgvsp: ENSP00000429527.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys135Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

8-82626244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626244
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 82626244
    reference: chr 8
allele count: 2
allele frequency: 1.665278934221482e-5
allele num: 120100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430719
  ensembl transcript: ENST00000520076
  gene symbol: ZFAND1
  hgvsc: ENST00000520076.1:c.68G>A
  hgvsp: ENSP00000430719.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427811
  ensembl transcript: ENST00000517450
  gene symbol: ZFAND1
  hgvsc: ENST00000517450.1:c.68G>A
  hgvsp: ENSP00000427811.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428927
  ensembl transcript: ENST00000523431
  gene symbol: ZFAND1
  hgvsc: ENST00000523431.1:c.68G>A
  hgvsp: ENSP00000428927.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429527
  ensembl transcript: ENST00000521895
  gene symbol: ZFAND1
  hgvsc: ENST00000521895.1:c.68G>A
  hgvsp: ENSP00000429527.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428375
  ensembl transcript: ENST00000519464
  gene symbol: ZFAND1
  hgvsc: ENST00000519464.1:c.389G>A
  hgvsp: ENSP00000428375.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430736
  ensembl transcript: ENST00000523096
  gene symbol: ZFAND1
  hgvsc: ENST00000523096.1:c.389G>A
  hgvsp: ENSP00000430736.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428101
  ensembl transcript: ENST00000520604
  gene symbol: ZFAND1
  hgvsc: ENST00000520604.1:c.68G>A
  hgvsp: ENSP00000428101.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430405
  ensembl transcript: ENST00000521742
  gene symbol: ZFAND1
  hgvsc: ENST00000521742.1:c.68G>A
  hgvsp: ENSP00000430405.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429167
  ensembl transcript: ENST00000519523
  gene symbol: ZFAND1
  hgvsc: ENST00000519523.1:c.389G>A
  hgvsp: ENSP00000429167.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000427957
  ensembl transcript: ENST00000523361
  gene symbol: ZFAND1
  hgvsc: ENST00000523361.1:c.68G>A
  hgvsp: ENSP00000427957.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430499
  ensembl transcript: ENST00000522032
  gene symbol: ZFAND1
  hgvsc: ENST00000522032.1:c.32G>A
  hgvsp: ENSP00000430499.1:p.Arg11Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000220669
  ensembl transcript: ENST00000220669
  gene symbol: ZFAND1
  hgvsc: ENST00000220669.5:c.389G>A
  hgvsp: ENSP00000220669.5:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000429999
  ensembl transcript: ENST00000522520
  gene symbol: ZFAND1
  hgvsc: ENST00000522520.1:c.68G>A
  hgvsp: ENSP00000429999.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104231
  ensembl transcript: ENST00000524305
  gene symbol: ZFAND1
  hgvsc: ENST00000524305.1:n.940G>A
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428278
  ensembl transcript: ENST00000520635
  gene symbol: ZFAND1
  hgvsc: ENST00000520635.1:c.68G>A
  hgvsp: ENSP00000428278.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428527
  ensembl transcript: ENST00000518419
  gene symbol: ZFAND1
  hgvsc: ENST00000518419.1:c.68G>A
  hgvsp: ENSP00000428527.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000430214
  ensembl transcript: ENST00000517588
  gene symbol: ZFAND1
  hgvsc: ENST00000517588.1:c.68G>A
  hgvsp: ENSP00000430214.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104231
  ensembl protein: ENSP00000428139
  ensembl transcript: ENST00000521287
  gene symbol: ZFAND1
  hgvsc: ENST00000521287.1:c.68G>A
  hgvsp: ENSP00000428139.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/25858
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg130Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-82626273-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82626273
allele count: 9
allele frequency: 7.666621234837127e-5
allele num: 117392
alternate allele: C
canonical: false
consequence: start lost
filter: PASS
hgvs: p.Asp1?
num of homozygotes: 0
reference allele: A

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

GenotypeDepth
all individuals: 198
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13178
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 295
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23755
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4466
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.452422993917991e-5
allele num: 40776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.58e0

DP
type: SiteQuality
SIO_000300: 9.0622e5

MQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.842e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.81e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

VQSLOD
type: SiteQuality
SIO_000300: -2.95e0

QD
type: SiteQuality
SIO_000300: 2.9e0

GenotypeDepth
all individuals: 18785
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18067
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22818
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.363884342607747e-4
allele num: 7332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.400845097474311e-5
allele num: 41652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.412429378531073e-3
allele num: 7788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 2.695e0

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.93e-1

DP
type: SiteQuality
SIO_000300: 9.27415e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

GenotypeDepth
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18067
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4478
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3680
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22818
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.400845097474311e-5
allele num: 41652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 2.695e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

DP
type: SiteQuality
SIO_000300: 9.27415e5

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeDepth
all individuals: 4020
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3290
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19907
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.223605799163924e-5
allele num: 44972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

DP
type: SiteQuality
SIO_000300: 9.979e5

FS
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

QD
type: SiteQuality
SIO_000300: 1.263e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

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

GenotypeDepth
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.333528894103843e-5
allele num: 13636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44972
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 14
allele frequency: 2.318648559125538e-3
allele num: 6038
num of homozygotes: 0

DP
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SIO_000300: 9.979e5

ReadPosRankSum
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SIO_000300: 5.580000000000001e-1

MQRankSum
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SIO_000300: 1.06e-1

BaseQRankSum
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FS
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SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -3.34e-1

InbreedingCoeff
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SIO_000300: 9.2e-3

VQSLOD
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SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.263e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.560531840447865e-5
allele num: 45728
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4924
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.613587087448808e-4
allele num: 8302
num of homozygotes: 0

South Asian
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allele count: 11
allele frequency: 7.989540964555491e-4
allele num: 13768
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.572e0

MQRankSum
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SIO_000300: 2.99e-1

ClippingRankSum
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SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.011174e6

InbreedingCoeff
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SIO_000300: -4.2e-3

BaseQRankSum
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SIO_000300: 2.38e0

QD
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SIO_000300: 1.17e1

ReadPosRankSum
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SIO_000300: -3.5e-2

VQSLOD
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SIO_000300: 2.14e0

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

South Asian
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allele frequency: 7.016559079427449e-5
allele num: 14252
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 3.51123595505618e-4
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 121
allele frequency: 2.482662398949485e-3
allele num: 48738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 7.648183556405354e-4
allele num: 5230
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.094e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

DP
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SIO_000300: 1.065955e6

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 2.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5316
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6670
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49440
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South 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: 3
allele frequency: 3.45701774602443e-4
allele num: 8678
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.745000000000001e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-3

BaseQRankSum
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QD
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DP
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SIO_000300: 1.079516e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 4.05e-1

FS
type: SiteQuality
SIO_000300: 9.77e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 2.084491384102279e-4
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num of homozygotes: 0

East Asian
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allele count: 16
allele frequency: 2.381661208693063e-3
allele num: 6718
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49860
num of homozygotes: 0

European (Finnish)
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allele count: 0
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African
type: Population
allele count: 2
allele frequency: 2.295684113865932e-4
allele num: 8712
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
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
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InbreedingCoeff
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SIO_000300: -2.7e-3

MQRankSum
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14474
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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Latino
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allele num: 8918
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 2.610625244746117e-4
allele num: 15322
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59716
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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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

VQSLOD
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
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allele count: 2
allele frequency: 1.823819077147547e-4
allele num: 10966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15398
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8284
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61278
num of homozygotes: 0

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

MQRankSum
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SIO_000300: 1.96e0

InbreedingCoeff
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VQSLOD
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DP
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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SIO_000300: -4.7e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61530
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.633939233116624e-5
allele num: 15074
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -1.809e0

InbreedingCoeff
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SIO_000300: -7.0e-4

ClippingRankSum
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SIO_000300: -4.93e-1

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.314098e6

VQSLOD
type: SiteQuality
SIO_000300: -6.944e-1

ReadPosRankSum
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SIO_000300: 0.0e0

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 6.68359844940516e-5
allele num: 14962
num of homozygotes: 0

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

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

African
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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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61618
num of homozygotes: 0

MQRankSum
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SIO_000300: -6.67e-1

QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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SIO_000300: 1.314904e6

FS
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -1.733e0

VQSLOD
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SIO_000300: -3.255e0

ClippingRankSum
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SIO_000300: 2.13e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 9216
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South Asian
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Latino
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allele frequency: 0.0e0
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DP
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 2.639772573439827e-3
allele num: 14774
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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East Asian
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 9.036688957166094e-5
allele num: 11066
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61218
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

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

QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 1.08e0

MQ
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.6e-3

FS
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DP
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ReadPosRankSum
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SIO_000300: -3.88e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.200192030724916e-4
allele num: 8332
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61098
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

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

VQSLOD
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SIO_000300: 1.67e-1

InbreedingCoeff
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SIO_000300: -1.6e-3

MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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SIO_000300: 1.297721e6

FS
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BaseQRankSum
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SIO_000300: 2.13e0

MQRankSum
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SIO_000300: -1.392e0

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 19
allele frequency: 3.152689742143165e-4
allele num: 60266
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.250731487733513e-4
allele num: 8886
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.515e0

InbreedingCoeff
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SIO_000300: -3.1e-3

QD
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SIO_000300: 1.104e1

VQSLOD
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SIO_000300: 1.72e0

MQRankSum
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DP
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MQ
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SIO_000300: 5.947e1

BaseQRankSum
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SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.95924864692773e-5
allele num: 12564
num of homozygotes: 0

African
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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
allele num: 778
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10818
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
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InbreedingCoeff
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SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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DP
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SIO_000300: 1.21688e6

FS
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SIO_000300: 8.451000000000001e0

MQRankSum
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SIO_000300: 1.71e0

BaseQRankSum
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SIO_000300: -2.062e0

VQSLOD
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SIO_000300: -2.008e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.540700350529335e-5
allele num: 56486
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 0
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Latino
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allele frequency: 0.0e0
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African
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VQSLOD
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QD
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Other
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Latino
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South Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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African
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European (Finnish)
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East Asian
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MQ
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MQRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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Other
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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FS
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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allele frequency: 5.555555555555556e-3
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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Latino
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 8484
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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Other
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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African
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East Asian
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Other
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European (Finnish)
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InbreedingCoeff
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QD
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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GenotypeQuality
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African
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European (Finnish)
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QD
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VQSLOD
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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DP
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MQ
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6795
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variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.175e1

FS
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 2.000449e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 303
bin: 8.75e1
variant carriers: 157

GenotypeDepth
all individuals: 614
bin: 5.75e1
variant carriers: 352

GenotypeDepth
all individuals: 570
bin: 6.25e1
variant carriers: 316

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 1183
bin: 4.25e1
variant carriers: 295

GenotypeDepth
all individuals: 311
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variant carriers: 166

GenotypeDepth
all individuals: 11587
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variant carriers: 125

GenotypeDepth
all individuals: 399
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variant carriers: 240

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 306

GenotypeDepth
all individuals: 2561
bin: 9.75e1
variant carriers: 889

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

GenotypeQuality
all individuals: 1476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
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variant carriers: 1

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 6546
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variant carriers: 1

GenotypeQuality
all individuals: 14
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variant carriers: 1

GenotypeQuality
all individuals: 9
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variant carriers: 1

GenotypeQuality
all individuals: 7
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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: 77
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 2

GenotypeQuality
all individuals: 1458
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variant carriers: 0

GenotypeQuality
all individuals: 8554
bin: 9.75e1
variant carriers: 4280

GenotypeQuality
all individuals: 40960
bin: 6.25e1
variant carriers: 3

Latino
type: Population
allele count: 229
allele frequency: 1.978572662865042e-2
allele num: 11574
num of homozygotes: 4

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

European (Non-Finnish)
type: Population
allele count: 3184
allele frequency: 4.776907612446365e-2
allele num: 66654
num of homozygotes: 73

European (Finnish)
type: Population
allele count: 143
allele frequency: 2.162734422262553e-2
allele num: 6612
num of homozygotes: 1

South Asian
type: Population
allele count: 731
allele frequency: 4.441608943978612e-2
allele num: 16458
num of homozygotes: 20

African
type: Population
allele count: 74
allele frequency: 7.116753221773418e-3
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 25
allele frequency: 2.753303964757709e-2
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 2.163963e6

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

QD
type: SiteQuality
SIO_000300: 1.264e1

FS
type: SiteQuality
SIO_000300: 1.204e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.594e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

GenotypeDepth
all individuals: 263
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
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variant carriers: 0

GenotypeDepth
all individuals: 277
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variant carriers: 0

GenotypeDepth
all individuals: 957
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variant carriers: 0

GenotypeDepth
all individuals: 356
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variant carriers: 0

GenotypeDepth
all individuals: 170
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variant carriers: 0

GenotypeDepth
all individuals: 25
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variant carriers: 0

GenotypeDepth
all individuals: 154
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variant carriers: 0

GenotypeDepth
all individuals: 158
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variant carriers: 0

GenotypeDepth
all individuals: 224
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 414
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variant carriers: 0

GenotypeQuality
all individuals: 1590
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 4589
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variant carriers: 1

GenotypeQuality
all individuals: 1607
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 43962
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variant carriers: 0

GenotypeQuality
all individuals: 906
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GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 7111
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.446e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.008e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 3.994e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.98176e6

GenotypeDepth
all individuals: 958
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2756
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variant carriers: 0

GenotypeDepth
all individuals: 277
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 12683
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variant carriers: 0

GenotypeDepth
all individuals: 27444
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variant carriers: 1

GenotypeDepth
all individuals: 1826
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variant carriers: 1

GenotypeDepth
all individuals: 12396
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variant carriers: 0

GenotypeDepth
all individuals: 16
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variant carriers: 0

GenotypeDepth
all individuals: 48
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GenotypeDepth
all individuals: 355
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variant carriers: 0

GenotypeDepth
all individuals: 154
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GenotypeDepth
all individuals: 169
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 350
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GenotypeQuality
all individuals: 4590
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variant carriers: 3

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 7116
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1603
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variant carriers: 0

GenotypeQuality
all individuals: 44002
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 414
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variant carriers: 0

GenotypeQuality
all individuals: 1594
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variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.821272462360369e-4
allele num: 16472
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: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
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: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.572e1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.982678e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 158
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12403
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variant carriers: 0

GenotypeDepth
all individuals: 263
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variant carriers: 0

GenotypeDepth
all individuals: 27450
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GenotypeDepth
all individuals: 154
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 2757
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GenotypeDepth
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GenotypeDepth
all individuals: 224
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GenotypeDepth
all individuals: 1828
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
all individuals: 582
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GenotypeQuality
all individuals: 906
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 3
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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: 6
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1594
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7118
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variant carriers: 0

GenotypeQuality
all individuals: 4588
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 414
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
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: 1.982855e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.169e1

GenotypeDepth
all individuals: 191
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 355
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 1828
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.982855e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
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SIO_000300: 3.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.169e1

GenotypeDepth
all individuals: 582
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variant carriers: 0

GenotypeDepth
all individuals: 27455
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variant carriers: 0

GenotypeDepth
all individuals: 277
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 12405
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variant carriers: 0

GenotypeDepth
all individuals: 2758
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variant carriers: 0

GenotypeDepth
all individuals: 5
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GenotypeDepth
all individuals: 49
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GenotypeDepth
all individuals: 30
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GenotypeDepth
all individuals: 1825
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variant carriers: 0

GenotypeDepth
all individuals: 154
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GenotypeDepth
all individuals: 224
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variant carriers: 0

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

European (Finnish)
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South Asian
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Latino
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Other
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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African
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Other
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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DP
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MQRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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SIO_000300: 6.77e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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African
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allele num: 10402
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European (Finnish)
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allele count: 0
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num of homozygotes: 0

Latino
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South Asian
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Other
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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num of homozygotes: 0

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

East Asian
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African
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South Asian
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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MQ
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VQSLOD
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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East Asian
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Latino
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.581e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.32e0

MQRankSum
type: SiteQuality
SIO_000300: -2.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

FS
type: SiteQuality
SIO_000300: 1.152e0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

DP
type: SiteQuality
SIO_000300: 1.974669e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 12259
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 950
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11647
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 345
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 620
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1825
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27243
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 607
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2736
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42707
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4541
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1501
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15702
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.553e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 1.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.963914e6