7-100364753-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364753
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364753
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4733A>T
  hgvsp: ENSP00000444427.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4733A>T
  hgvsp: ENSP00000425454.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4733A>T
  hgvsp: ENSP00000421245.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4733A>T
  hgvsp: ENSP00000425200.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4733A>T
  hgvsp: ENSP00000422387.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4733A>T
  hgvsp: ENSP00000423579.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4733A>T
  hgvsp: ENSP00000445943.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4733A>T
  hgvsp: ENSP00000422208.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4733A>T
  hgvsp: ENSP00000445091.1:p.Asp1578Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.464A>T
  hgvsp: ENSP00000441117.1:p.Asp155Val
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp1578Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/7-100364755-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364755
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364755
    reference: chr 7
allele count: 17
allele frequency: 1.408427366572219e-4
allele num: 120702
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4735A>C
  hgvsp: ENSP00000445943.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4735A>C
  hgvsp: ENSP00000425200.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4735A>C
  hgvsp: ENSP00000444427.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4735A>C
  hgvsp: ENSP00000423579.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4735A>C
  hgvsp: ENSP00000425454.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4735A>C
  hgvsp: ENSP00000421245.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.466A>C
  hgvsp: ENSP00000441117.1:p.Ser156Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4735A>C
  hgvsp: ENSP00000422208.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4735A>C
  hgvsp: ENSP00000422387.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4735A>C
  hgvsp: ENSP00000445091.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13981
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser1579Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

7-100364757-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364757
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364757
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.468C>G
  hgvsp: ENSP00000441117.1:p.Ser156Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4737C>G
  hgvsp: ENSP00000425200.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4737C>G
  hgvsp: ENSP00000421245.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4737C>G
  hgvsp: ENSP00000444427.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4737C>G
  hgvsp: ENSP00000425454.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4737C>G
  hgvsp: ENSP00000445943.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4737C>G
  hgvsp: ENSP00000422387.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4737C>G
  hgvsp: ENSP00000422208.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4737C>G
  hgvsp: ENSP00000423579.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4737C>G
  hgvsp: ENSP00000445091.1:p.Ser1579Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13982
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser1579Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

7-100364760-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364760
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364760
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4740T>G
  hgvsp: ENSP00000422387.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4740T>G
  hgvsp: ENSP00000425454.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.471T>G
  hgvsp: ENSP00000441117.1:p.Tyr157Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4740T>G
  hgvsp: ENSP00000421245.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4740T>G
  hgvsp: ENSP00000444427.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4740T>G
  hgvsp: ENSP00000425200.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4740T>G
  hgvsp: ENSP00000422208.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4740T>G
  hgvsp: ENSP00000445943.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4740T>G
  hgvsp: ENSP00000423579.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4740T>G
  hgvsp: ENSP00000445091.1:p.Tyr1580Ter
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11650
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21814
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr1580Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-100364763-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364763
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364763
    reference: chr 7
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4743T>G
  hgvsp: ENSP00000444427.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4743T>G
  hgvsp: ENSP00000422208.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4743T>G
  hgvsp: ENSP00000423579.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4743T>G
  hgvsp: ENSP00000421245.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4743T>G
  hgvsp: ENSP00000445091.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4743T>G
  hgvsp: ENSP00000422387.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4743T>G
  hgvsp: ENSP00000445943.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.474T>G
  hgvsp: ENSP00000441117.1:p.Phe158Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4743T>G
  hgvsp: ENSP00000425200.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4743T>G
  hgvsp: ENSP00000425454.1:p.Phe1581Leu
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe1581Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-100364767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364767
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364767
    reference: chr 7
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.478G>A
  hgvsp: ENSP00000441117.1:p.Val160Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4747G>A
  hgvsp: ENSP00000425454.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4747G>A
  hgvsp: ENSP00000445943.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4747G>A
  hgvsp: ENSP00000422387.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4747G>A
  hgvsp: ENSP00000422208.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4747G>A
  hgvsp: ENSP00000444427.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4747G>A
  hgvsp: ENSP00000421245.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4747G>A
  hgvsp: ENSP00000445091.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4747G>A
  hgvsp: ENSP00000423579.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4747G>A
  hgvsp: ENSP00000425200.1:p.Val1583Met
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5921
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val1583Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

7-100364769-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364769
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364769
    reference: chr 7
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4749G>T
  hgvsp: ENST00000443370.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4749G>T
  hgvsp: ENST00000421100.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4749G>T
  hgvsp: ENST00000542585.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.480G>T
  hgvsp: ENST00000546213.1:c.480G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4749G>T
  hgvsp: ENST00000449052.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4749G>T
  hgvsp: ENST00000427578.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4749G>T
  hgvsp: ENST00000546292.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4749G>T
  hgvsp: ENST00000348028.3:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4749G>T
  hgvsp: ENST00000349350.6:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4749G>T
  hgvsp: ENST00000538115.1:c.4749G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val1583Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-100364769-GAGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364769
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364766
    reference: chr 7
allele count: 3
allele frequency: 2.48541887592789e-5
allele num: 120704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.481_483delAGC
  hgvsp: ENSP00000441117.1:p.Ser161del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4750_4752delAGC
  hgvsp: ENSP00000445091.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4750_4752delAGC
  hgvsp: ENSP00000422387.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4750_4752delAGC
  hgvsp: ENSP00000421245.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4750_4752delAGC
  hgvsp: ENSP00000425454.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4750_4752delAGC
  hgvsp: ENSP00000445943.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4750_4752delAGC
  hgvsp: ENSP00000444427.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4750_4752delAGC
  hgvsp: ENSP00000425200.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4750_4752delAGC
  hgvsp: ENSP00000422208.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4750_4752delAGC
  hgvsp: ENSP00000423579.1:p.Ser1584del
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser1584del
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GAGC
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

7-100364771-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364771
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364771
    reference: chr 7
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4751G>A
  hgvsp: ENSP00000423579.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4751G>A
  hgvsp: ENSP00000421245.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4751G>A
  hgvsp: ENSP00000444427.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.482G>A
  hgvsp: ENSP00000441117.1:p.Ser161Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4751G>A
  hgvsp: ENSP00000425200.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4751G>A
  hgvsp: ENSP00000422387.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4751G>A
  hgvsp: ENSP00000422208.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4751G>A
  hgvsp: ENSP00000425454.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4751G>A
  hgvsp: ENSP00000445943.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4751G>A
  hgvsp: ENSP00000445091.1:p.Ser1584Asn
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser1584Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

7-100364772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364772
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364772
    reference: chr 7
allele count: 9
allele frequency: 7.456503728251864e-5
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4752C>T
  hgvsp: ENST00000538115.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4752C>T
  hgvsp: ENST00000348028.3:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4752C>T
  hgvsp: ENST00000427578.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4752C>T
  hgvsp: ENST00000443370.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4752C>T
  hgvsp: ENST00000546292.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4752C>T
  hgvsp: ENST00000349350.6:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4752C>T
  hgvsp: ENST00000449052.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.483C>T
  hgvsp: ENST00000546213.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4752C>T
  hgvsp: ENST00000542585.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4752C>T
  hgvsp: ENST00000421100.1:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser1584Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

7-100364773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364773
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364773
    reference: chr 7
allele count: 4
allele frequency: 3.314166404295159e-5
allele num: 120694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.484G>A
  hgvsp: ENSP00000441117.1:p.Ala162Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4753G>A
  hgvsp: ENSP00000425454.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4753G>A
  hgvsp: ENSP00000421245.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4753G>A
  hgvsp: ENSP00000444427.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4753G>A
  hgvsp: ENSP00000445091.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4753G>A
  hgvsp: ENSP00000422208.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4753G>A
  hgvsp: ENSP00000423579.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4753G>A
  hgvsp: ENSP00000445943.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4753G>A
  hgvsp: ENSP00000422387.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4753G>A
  hgvsp: ENSP00000425200.1:p.Ala1585Thr
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala1585Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-100364780-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364780
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364780
    reference: chr 7
allele count: 6
allele frequency: 4.971414367387522e-5
allele num: 120690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4760A>C
  hgvsp: ENSP00000444427.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4760A>C
  hgvsp: ENSP00000423579.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4760A>C
  hgvsp: ENSP00000425454.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4760A>C
  hgvsp: ENSP00000425200.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4760A>C
  hgvsp: ENSP00000422208.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4760A>C
  hgvsp: ENSP00000445091.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4760A>C
  hgvsp: ENSP00000445943.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4760A>C
  hgvsp: ENSP00000422387.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4760A>C
  hgvsp: ENSP00000421245.1:p.Asn1587Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.491A>C
  hgvsp: ENSP00000441117.1:p.Asn164Thr
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn1587Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

7-100364780-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364780
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364780
    reference: chr 7
allele count: 3
allele frequency: 2.485707183693761e-5
allele num: 120690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4760A>G
  hgvsp: ENSP00000445091.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4760A>G
  hgvsp: ENSP00000422387.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4760A>G
  hgvsp: ENSP00000422208.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.491A>G
  hgvsp: ENSP00000441117.1:p.Asn164Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4760A>G
  hgvsp: ENSP00000444427.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4760A>G
  hgvsp: ENSP00000445943.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4760A>G
  hgvsp: ENSP00000425454.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4760A>G
  hgvsp: ENSP00000421245.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4760A>G
  hgvsp: ENSP00000423579.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4760A>G
  hgvsp: ENSP00000425200.1:p.Asn1587Ser
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn1587Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

7-100364781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364781
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364781
    reference: chr 7
allele count: 2
allele frequency: 1.657220509761029e-5
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4761C>T
  hgvsp: ENST00000449052.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4761C>T
  hgvsp: ENST00000542585.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4761C>T
  hgvsp: ENST00000349350.6:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4761C>T
  hgvsp: ENST00000546292.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4761C>T
  hgvsp: ENST00000443370.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4761C>T
  hgvsp: ENST00000348028.3:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4761C>T
  hgvsp: ENST00000421100.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.492C>T
  hgvsp: ENST00000546213.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4761C>T
  hgvsp: ENST00000427578.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4761C>T
  hgvsp: ENST00000538115.1:c.4761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21786
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Asn1587Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

7-100364782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364782
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364782
    reference: chr 7
allele count: 4
allele frequency: 3.314495948028704e-5
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4762G>A
  hgvsp: ENSP00000445091.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4762G>A
  hgvsp: ENSP00000421245.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4762G>A
  hgvsp: ENSP00000444427.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4762G>A
  hgvsp: ENSP00000422387.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.493G>A
  hgvsp: ENSP00000441117.1:p.Glu165Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4762G>A
  hgvsp: ENSP00000422208.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4762G>A
  hgvsp: ENSP00000445943.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4762G>A
  hgvsp: ENSP00000425454.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4762G>A
  hgvsp: ENSP00000423579.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4762G>A
  hgvsp: ENSP00000425200.1:p.Glu1588Lys
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu1588Lys
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

7-100364788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364788
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364788
    reference: chr 7
allele count: 28
allele frequency: 2.320531733271452e-4
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4768C>T
  hgvsp: ENSP00000422387.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4768C>T
  hgvsp: ENSP00000425454.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4768C>T
  hgvsp: ENSP00000425200.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.499C>T
  hgvsp: ENSP00000441117.1:p.Arg167Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4768C>T
  hgvsp: ENSP00000421245.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4768C>T
  hgvsp: ENSP00000423579.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4768C>T
  hgvsp: ENSP00000445091.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4768C>T
  hgvsp: ENSP00000445943.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4768C>T
  hgvsp: ENSP00000422208.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4768C>T
  hgvsp: ENSP00000444427.1:p.Arg1590Cys
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7570
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1590Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-100364789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364789
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364789
    reference: chr 7
allele count: 6
allele frequency: 4.972403162448411e-5
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.500G>A
  hgvsp: ENSP00000441117.1:p.Arg167His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4769G>A
  hgvsp: ENSP00000445943.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4769G>A
  hgvsp: ENSP00000445091.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4769G>A
  hgvsp: ENSP00000422387.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4769G>A
  hgvsp: ENSP00000421245.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4769G>A
  hgvsp: ENSP00000425454.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4769G>A
  hgvsp: ENSP00000423579.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4769G>A
  hgvsp: ENSP00000444427.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4769G>A
  hgvsp: ENSP00000425200.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4769G>A
  hgvsp: ENSP00000422208.1:p.Arg1590His
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1590His
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-100364789-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364789
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364789
    reference: chr 7
allele count: 7
allele frequency: 5.80113702285648e-5
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4769G>T
  hgvsp: ENSP00000445943.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4769G>T
  hgvsp: ENSP00000422208.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4769G>T
  hgvsp: ENSP00000425454.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4769G>T
  hgvsp: ENSP00000422387.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4769G>T
  hgvsp: ENSP00000445091.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4769G>T
  hgvsp: ENSP00000421245.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4769G>T
  hgvsp: ENSP00000444427.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4769G>T
  hgvsp: ENSP00000423579.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4769G>T
  hgvsp: ENSP00000425200.1:p.Arg1590Leu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.500G>T
  hgvsp: ENSP00000441117.1:p.Arg167Leu
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg1590Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

7-100364790-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364790
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364791
    reference: chr 7
allele count: 2
allele frequency: 1.657769967839263e-5
allele num: 120644
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4776dupG
  hgvsp: ENSP00000444427.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4776dupG
  hgvsp: ENSP00000425200.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4776dupG
  hgvsp: ENSP00000422387.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.507dupG
  hgvsp: ENSP00000441117.1:p.Ile170AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4776dupG
  hgvsp: ENSP00000423579.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4776dupG
  hgvsp: ENSP00000425454.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4776dupG
  hgvsp: ENSP00000421245.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4776dupG
  hgvsp: ENSP00000445091.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4776dupG
  hgvsp: ENSP00000422208.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4776dupG
  hgvsp: ENSP00000445943.1:p.Ile1593AspfsTer16
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5850
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile1593AspfsTer16
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-100364790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364790
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364790
    reference: chr 7
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4770C>T
  hgvsp: ENST00000348028.3:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4770C>T
  hgvsp: ENST00000349350.6:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4770C>T
  hgvsp: ENST00000538115.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4770C>T
  hgvsp: ENST00000427578.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4770C>T
  hgvsp: ENST00000421100.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4770C>T
  hgvsp: ENST00000443370.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4770C>T
  hgvsp: ENST00000542585.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4770C>T
  hgvsp: ENST00000546292.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.501C>T
  hgvsp: ENST00000546213.1:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4770C>T
  hgvsp: ENST00000449052.1:c.4770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13836
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg1590Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

7-100364791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364791
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364791
    reference: chr 7
allele count: 5
allele frequency: 4.145043357153516e-5
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.502G>A
  hgvsp: ENSP00000441117.1:p.Gly168Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4771G>A
  hgvsp: ENSP00000445091.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4771G>A
  hgvsp: ENSP00000444427.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4771G>A
  hgvsp: ENSP00000421245.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4771G>A
  hgvsp: ENSP00000422387.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4771G>A
  hgvsp: ENSP00000423579.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4771G>A
  hgvsp: ENSP00000445943.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4771G>A
  hgvsp: ENSP00000422208.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4771G>A
  hgvsp: ENSP00000425454.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4771G>A
  hgvsp: ENSP00000425200.1:p.Gly1591Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly1591Arg
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: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

7-100364794-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364794
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364794
    reference: chr 7
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4774G>A
  hgvsp: ENSP00000423579.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4774G>A
  hgvsp: ENSP00000422387.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4774G>A
  hgvsp: ENSP00000444427.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4774G>A
  hgvsp: ENSP00000421245.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4774G>A
  hgvsp: ENSP00000445091.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.505G>A
  hgvsp: ENSP00000441117.1:p.Gly169Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4774G>A
  hgvsp: ENSP00000425200.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4774G>A
  hgvsp: ENSP00000422208.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4774G>A
  hgvsp: ENSP00000425454.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4774G>A
  hgvsp: ENSP00000445943.1:p.Gly1592Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly1592Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

7-100364796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364796
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364796
    reference: chr 7
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4776G>A
  hgvsp: ENST00000421100.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4776G>A
  hgvsp: ENST00000443370.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4776G>A
  hgvsp: ENST00000427578.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4776G>A
  hgvsp: ENST00000538115.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4776G>A
  hgvsp: ENST00000348028.3:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4776G>A
  hgvsp: ENST00000349350.6:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.507G>A
  hgvsp: ENST00000546213.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4776G>A
  hgvsp: ENST00000546292.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4776G>A
  hgvsp: ENST00000542585.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4776G>A
  hgvsp: ENST00000449052.1:c.4776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly1592Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

7-100364796-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364796
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364796
    reference: chr 7
allele count: 2
allele frequency: 1.657632569164719e-5
allele num: 120654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.507G>T
  hgvsp: ENST00000546213.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4776G>T
  hgvsp: ENST00000421100.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4776G>T
  hgvsp: ENST00000349350.6:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4776G>T
  hgvsp: ENST00000546292.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4776G>T
  hgvsp: ENST00000443370.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4776G>T
  hgvsp: ENST00000542585.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4776G>T
  hgvsp: ENST00000427578.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4776G>T
  hgvsp: ENST00000538115.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4776G>T
  hgvsp: ENST00000449052.1:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4776G>T
  hgvsp: ENST00000348028.3:c.4776G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21730
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly1592Gly
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

7-100364797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364797
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364797
    reference: chr 7
allele count: 270
allele frequency: 2.237841063554686e-3
allele num: 120652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4777A>G
  hgvsp: ENSP00000425454.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4777A>G
  hgvsp: ENSP00000444427.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4777A>G
  hgvsp: ENSP00000422208.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.508A>G
  hgvsp: ENSP00000441117.1:p.Ile170Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4777A>G
  hgvsp: ENSP00000422387.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4777A>G
  hgvsp: ENSP00000425200.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4777A>G
  hgvsp: ENSP00000423579.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4777A>G
  hgvsp: ENSP00000421245.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4777A>G
  hgvsp: ENSP00000445943.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4777A>G
  hgvsp: ENSP00000445091.1:p.Ile1593Val
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10700
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11604
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.75e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 3226
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile1593Val
num of homozygotes: 8
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-100364807-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364807
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364807
    reference: chr 7
allele count: 20
allele frequency: 1.658072325114821e-4
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4787T>C
  hgvsp: ENSP00000444427.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4787T>C
  hgvsp: ENSP00000445943.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4787T>C
  hgvsp: ENSP00000445091.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4787T>C
  hgvsp: ENSP00000423579.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4787T>C
  hgvsp: ENSP00000425454.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.518T>C
  hgvsp: ENSP00000441117.1:p.Val173Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4787T>C
  hgvsp: ENSP00000422387.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4787T>C
  hgvsp: ENSP00000421245.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4787T>C
  hgvsp: ENSP00000425200.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4787T>C
  hgvsp: ENSP00000422208.1:p.Val1596Ala
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11696
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val1596Ala
num of homozygotes: 1
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-100364812-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364812
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364812
    reference: chr 7
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4792T>G
  hgvsp: ENSP00000423579.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4792T>G
  hgvsp: ENSP00000425454.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4792T>G
  hgvsp: ENSP00000421245.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.523T>G
  hgvsp: ENSP00000441117.1:p.Tyr175Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4792T>G
  hgvsp: ENSP00000422208.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4792T>G
  hgvsp: ENSP00000422387.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4792T>G
  hgvsp: ENSP00000444427.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4792T>G
  hgvsp: ENSP00000445091.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4792T>G
  hgvsp: ENSP00000445943.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4792T>G
  hgvsp: ENSP00000425200.1:p.Tyr1598Asp
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14144
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr1598Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS

7-100364823-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364823
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364823
    reference: chr 7
allele count: 4
allele frequency: 3.318730917297226e-5
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4803C>T
  hgvsp: ENST00000348028.3:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4803C>T
  hgvsp: ENST00000546292.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4803C>T
  hgvsp: ENST00000443370.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4803C>T
  hgvsp: ENST00000542585.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4803C>T
  hgvsp: ENST00000421100.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4803C>T
  hgvsp: ENST00000349350.6:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4803C>T
  hgvsp: ENST00000427578.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.534C>T
  hgvsp: ENST00000546213.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4803C>T
  hgvsp: ENST00000449052.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4803C>T
  hgvsp: ENST00000538115.1:c.4803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13990
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala1601Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

7-100364824-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364824
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364824
    reference: chr 7
allele count: 2
allele frequency: 1.65953068472236e-5
allele num: 120516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4804G>A
  hgvsp: ENSP00000422387.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4804G>A
  hgvsp: ENSP00000425200.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4804G>A
  hgvsp: ENSP00000444427.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.535G>A
  hgvsp: ENSP00000441117.1:p.Val179Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4804G>A
  hgvsp: ENSP00000423579.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4804G>A
  hgvsp: ENSP00000421245.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4804G>A
  hgvsp: ENSP00000445091.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4804G>A
  hgvsp: ENSP00000445943.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4804G>A
  hgvsp: ENSP00000425454.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4804G>A
  hgvsp: ENSP00000422208.1:p.Val1602Ile
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1602Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

7-100364829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364829
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364829
    reference: chr 7
allele count: 5
allele frequency: 4.150548702538475e-5
allele num: 120466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4809C>T
  hgvsp: ENST00000443370.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4809C>T
  hgvsp: ENST00000348028.3:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4809C>T
  hgvsp: ENST00000538115.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.540C>T
  hgvsp: ENST00000546213.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4809C>T
  hgvsp: ENST00000421100.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4809C>T
  hgvsp: ENST00000546292.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4809C>T
  hgvsp: ENST00000449052.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4809C>T
  hgvsp: ENST00000349350.6:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4809C>T
  hgvsp: ENST00000542585.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4809C>T
  hgvsp: ENST00000427578.1:c.4809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His1603His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-100364830-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364830
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364830
    reference: chr 7
allele count: 6
allele frequency: 4.981568197668626e-5
allele num: 120444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4810G>A
  hgvsp: ENSP00000445091.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4810G>A
  hgvsp: ENSP00000425454.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.541G>A
  hgvsp: ENSP00000441117.1:p.Val181Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4810G>A
  hgvsp: ENSP00000423579.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4810G>A
  hgvsp: ENSP00000422208.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4810G>A
  hgvsp: ENSP00000425200.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4810G>A
  hgvsp: ENSP00000422387.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4810G>A
  hgvsp: ENSP00000421245.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4810G>A
  hgvsp: ENSP00000445943.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4810G>A
  hgvsp: ENSP00000444427.1:p.Val1604Met
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val1604Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

7-100364834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364834
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364834
    reference: chr 7
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4814C>T
  hgvsp: ENSP00000422208.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4814C>T
  hgvsp: ENSP00000445091.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4814C>T
  hgvsp: ENSP00000423579.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4814C>T
  hgvsp: ENSP00000444427.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4814C>T
  hgvsp: ENSP00000425200.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.545C>T
  hgvsp: ENSP00000441117.1:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4814C>T
  hgvsp: ENSP00000421245.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4814C>T
  hgvsp: ENSP00000445943.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4814C>T
  hgvsp: ENSP00000422387.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4814C>T
  hgvsp: ENSP00000425454.1:p.Thr1605Ile
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr1605Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/7-100364834-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364834
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364833
    reference: chr 7
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4815delA
  hgvsp: ENSP00000425454.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.546delA
  hgvsp: ENSP00000441117.1:p.Val183SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4815delA
  hgvsp: ENSP00000425200.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4815delA
  hgvsp: ENSP00000422387.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4815delA
  hgvsp: ENSP00000445091.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4815delA
  hgvsp: ENSP00000445943.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4815delA
  hgvsp: ENSP00000422208.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4815delA
  hgvsp: ENSP00000421245.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4815delA
  hgvsp: ENSP00000444427.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4815delA
  hgvsp: ENSP00000423579.1:p.Val1606SerfsTer16
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val1606SerfsTer16
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: CA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

7-100364838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364838
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364838
    reference: chr 7
allele count: 3
allele frequency: 2.493724127612176e-5
allele num: 120302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4818C>T
  hgvsp: ENST00000427578.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4818C>T
  hgvsp: ENST00000349350.6:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4818C>T
  hgvsp: ENST00000443370.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4818C>T
  hgvsp: ENST00000449052.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4818C>T
  hgvsp: ENST00000538115.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4818C>T
  hgvsp: ENST00000421100.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4818C>T
  hgvsp: ENST00000546292.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4818C>T
  hgvsp: ENST00000348028.3:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.549C>T
  hgvsp: ENST00000546213.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4818C>T
  hgvsp: ENST00000542585.1:c.4818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1606Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/7-100364845-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364845
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364845
    reference: chr 7
allele count: 1
allele frequency: 8.327365388138501e-6
allele num: 120086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4825C>A
  hgvsp: ENSP00000421245.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4825C>A
  hgvsp: ENSP00000422387.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4825C>A
  hgvsp: ENSP00000445091.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4825C>A
  hgvsp: ENSP00000423579.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4825C>A
  hgvsp: ENSP00000425200.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4825C>A
  hgvsp: ENSP00000444427.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4825C>A
  hgvsp: ENSP00000425454.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.556C>A
  hgvsp: ENSP00000441117.1:p.Leu186Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4825C>A
  hgvsp: ENSP00000445943.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4825C>A
  hgvsp: ENSP00000422208.1:p.Leu1609Ile
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu1609Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-100364851-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364851
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364851
    reference: chr 7
allele count: 1
allele frequency: 8.331944675887353e-6
allele num: 120020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4831A>T
  hgvsp: ENSP00000445091.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.562A>T
  hgvsp: ENSP00000441117.1:p.Ile188Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4831A>T
  hgvsp: ENSP00000422208.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4831A>T
  hgvsp: ENSP00000421245.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4831A>T
  hgvsp: ENSP00000423579.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4831A>T
  hgvsp: ENSP00000425200.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4831A>T
  hgvsp: ENSP00000425454.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4831A>T
  hgvsp: ENSP00000422387.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4831A>T
  hgvsp: ENSP00000445943.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4831A>T
  hgvsp: ENSP00000444427.1:p.Ile1611Phe
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5609
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile1611Phe
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-100364851-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364851
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364850
    reference: chr 7
allele count: 40
allele frequency: 3.332777870354941e-4
allele num: 120020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4832delT
  hgvsp: ENSP00000445091.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4832delT
  hgvsp: ENSP00000425454.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4832delT
  hgvsp: ENSP00000444427.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4832delT
  hgvsp: ENSP00000425200.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4832delT
  hgvsp: ENSP00000421245.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4832delT
  hgvsp: ENSP00000423579.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4832delT
  hgvsp: ENSP00000422208.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.563delT
  hgvsp: ENSP00000441117.1:p.Ile188ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4832delT
  hgvsp: ENSP00000445943.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4832delT
  hgvsp: ENSP00000422387.1:p.Ile1611ThrfsTer11
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile1611ThrfsTer11
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: AT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

7-100364902-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364902
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364902
    reference: chr 7
allele count: 1
allele frequency: 8.663409224798143e-6
allele num: 115428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.591+22C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4860+22C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

7-100364911-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364911
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364911
    reference: chr 7
allele count: 3
allele frequency: 2.621873415951478e-5
allele num: 114422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.591+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4860+31T>C
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-100364919-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364919
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364919
    reference: chr 7
allele count: 9
allele frequency: 7.93846805207635e-5
allele num: 113372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.591+39C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4860+39C>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-100364921-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364921
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364921
    reference: chr 7
allele count: 19
allele frequency: 1.67903852951573e-4
allele num: 113160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.591+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4860+41G>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

7-100364922-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100364922
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100364922
    reference: chr 7
allele count: 1
allele frequency: 8.848774444739404e-6
allele num: 113010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.591+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4860+42C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9026
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-100365405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365405
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365405
    reference: chr 7
allele count: 1
allele frequency: 9.086943879034603e-6
allele num: 110048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-49C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5499
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-100365406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365406
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365406
    reference: chr 7
allele count: 1
allele frequency: 9.079518422342878e-6
allele num: 110138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-48C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-48C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4275
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS

7-100365407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365407
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365407
    reference: chr 7
allele count: 3
allele frequency: 2.72841370027466e-5
allele num: 109954
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-47C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16899
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-100365421-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365421
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365421
    reference: chr 7
allele count: 1
allele frequency: 8.987956138774043e-6
allele num: 111260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-33A>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-33A>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

7-100365422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365422
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365422
    reference: chr 7
allele count: 2
allele frequency: 1.794655515873728e-5
allele num: 111442
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-32C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-32C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-100365424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365424
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365424
    reference: chr 7
allele count: 1
allele frequency: 8.949186518945427e-6
allele num: 111742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-30C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-100365426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365426
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365426
    reference: chr 7
allele count: 1
allele frequency: 8.92920922923066e-6
allele num: 111992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-28C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

7-100365427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365427
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365427
    reference: chr 7
allele count: 1
allele frequency: 8.920924921495861e-6
allele num: 112096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-27C>G
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 26954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4068
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2803
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

7-100365434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365434
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365434
    reference: chr 7
allele count: 2
allele frequency: 1.770068147623683e-5
allele num: 112990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-20C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28565
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32696
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

7-100365435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365435
    reference: chr 7
allele count: 5300
allele frequency: 4.638624866530133e-2
allele num: 114258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-19G>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 1.25e1
  variant carriers: 349
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.75e1
  variant carriers: 574
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.75e1
  variant carriers: 650
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 511
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 27077
  bin: 2.25e1
  variant carriers: 641
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.5e0
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 3.25e1
  variant carriers: 800
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 15052
  bin: 2.75e1
  variant carriers: 744
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 31087
  bin: 6.25e1
  variant carriers: 21
num of homozygotes: 186
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/7-100365437-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365437
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365437
    reference: chr 7
allele count: 1
allele frequency: 8.72280665026779e-6
allele num: 114642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-17C>A
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-17C>A
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7055
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

7-100365446-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365446
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365446
    reference: chr 7
allele count: 1
allele frequency: 8.58236495648741e-6
allele num: 116518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4861-8C>T
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.592-8C>T
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
hgvs: c.4861-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-100365463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365463
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365463
    reference: chr 7
allele count: 1
allele frequency: 8.440100605999223e-6
allele num: 118482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4870C>T
  hgvsp: ENSP00000422387.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4870C>T
  hgvsp: ENSP00000423579.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.601C>T
  hgvsp: ENSP00000441117.1:p.His201Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4870C>T
  hgvsp: ENSP00000445943.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4870C>T
  hgvsp: ENSP00000421245.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4870C>T
  hgvsp: ENSP00000425200.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4870C>T
  hgvsp: ENSP00000425454.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4870C>T
  hgvsp: ENSP00000422208.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4870C>T
  hgvsp: ENSP00000444427.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4870C>T
  hgvsp: ENSP00000445091.1:p.His1624Tyr
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His1624Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

7-100365466-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365466
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365466
    reference: chr 7
allele count: 1
allele frequency: 8.422471153036301e-6
allele num: 118730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4873C>G
  hgvsp: ENSP00000445091.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4873C>G
  hgvsp: ENSP00000445943.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4873C>G
  hgvsp: ENSP00000421245.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4873C>G
  hgvsp: ENSP00000422208.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4873C>G
  hgvsp: ENSP00000422387.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4873C>G
  hgvsp: ENSP00000444427.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4873C>G
  hgvsp: ENSP00000425200.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4873C>G
  hgvsp: ENSP00000423579.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.604C>G
  hgvsp: ENSP00000441117.1:p.Arg202Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4873C>G
  hgvsp: ENSP00000425454.1:p.Arg1625Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1625Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

7-100365466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365466
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365466
    reference: chr 7
allele count: 8
allele frequency: 6.73797692242904e-5
allele num: 118730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4873C>T
  hgvsp: ENSP00000425454.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4873C>T
  hgvsp: ENSP00000425200.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4873C>T
  hgvsp: ENSP00000422208.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4873C>T
  hgvsp: ENSP00000444427.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4873C>T
  hgvsp: ENSP00000421245.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4873C>T
  hgvsp: ENSP00000422387.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.604C>T
  hgvsp: ENSP00000441117.1:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4873C>T
  hgvsp: ENSP00000445943.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4873C>T
  hgvsp: ENSP00000445091.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4873C>T
  hgvsp: ENSP00000423579.1:p.Arg1625Trp
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18069
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg1625Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-100365467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365467
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365467
    reference: chr 7
allele count: 215
allele frequency: 1.807330195023537e-3
allele num: 118960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.605G>A
  hgvsp: ENSP00000441117.1:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4874G>A
  hgvsp: ENSP00000423579.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4874G>A
  hgvsp: ENSP00000445091.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4874G>A
  hgvsp: ENSP00000421245.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4874G>A
  hgvsp: ENSP00000445943.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4874G>A
  hgvsp: ENSP00000444427.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4874G>A
  hgvsp: ENSP00000425454.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4874G>A
  hgvsp: ENSP00000422387.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4874G>A
  hgvsp: ENSP00000422208.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4874G>A
  hgvsp: ENSP00000425200.1:p.Arg1625Gln
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30072
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18100
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Arg1625Gln
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: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

7-100365471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365471
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365471
    reference: chr 7
allele count: 1
allele frequency: 8.38940250675347e-6
allele num: 119198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4878G>A
  hgvsp: ENST00000349350.6:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4878G>A
  hgvsp: ENST00000449052.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4878G>A
  hgvsp: ENST00000421100.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4878G>A
  hgvsp: ENST00000443370.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4878G>A
  hgvsp: ENST00000538115.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4878G>A
  hgvsp: ENST00000542585.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4878G>A
  hgvsp: ENST00000546292.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4878G>A
  hgvsp: ENST00000348028.3:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.609G>A
  hgvsp: ENST00000546213.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4878G>A
  hgvsp: ENST00000427578.1:c.4878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val1626Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

7-100365493-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365493
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365493
    reference: chr 7
allele count: 2
allele frequency: 1.664364296057121e-5
allele num: 120166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4900C>G
  hgvsp: ENSP00000444427.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4900C>G
  hgvsp: ENSP00000422387.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.631C>G
  hgvsp: ENSP00000441117.1:p.Gln211Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4900C>G
  hgvsp: ENSP00000425454.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4900C>G
  hgvsp: ENSP00000425200.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4900C>G
  hgvsp: ENSP00000422208.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4900C>G
  hgvsp: ENSP00000423579.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4900C>G
  hgvsp: ENSP00000421245.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4900C>G
  hgvsp: ENSP00000445943.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4900C>G
  hgvsp: ENSP00000445091.1:p.Gln1634Glu
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18889
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln1634Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-100365494-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365494
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365494
    reference: chr 7
allele count: 2
allele frequency: 1.663755095249979e-5
allele num: 120210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4901A>G
  hgvsp: ENSP00000444427.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4901A>G
  hgvsp: ENSP00000422208.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4901A>G
  hgvsp: ENSP00000425454.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4901A>G
  hgvsp: ENSP00000425200.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4901A>G
  hgvsp: ENSP00000445943.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4901A>G
  hgvsp: ENSP00000422387.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4901A>G
  hgvsp: ENSP00000421245.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4901A>G
  hgvsp: ENSP00000445091.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.632A>G
  hgvsp: ENSP00000441117.1:p.Gln211Arg
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4901A>G
  hgvsp: ENSP00000423579.1:p.Gln1634Arg
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7913
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln1634Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

7-100365498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365498
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365498
    reference: chr 7
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.636C>T
  hgvsp: ENST00000546213.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4905C>T
  hgvsp: ENST00000349350.6:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4905C>T
  hgvsp: ENST00000443370.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4905C>T
  hgvsp: ENST00000348028.3:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4905C>T
  hgvsp: ENST00000542585.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4905C>T
  hgvsp: ENST00000421100.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4905C>T
  hgvsp: ENST00000427578.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4905C>T
  hgvsp: ENST00000546292.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4905C>T
  hgvsp: ENST00000538115.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4905C>T
  hgvsp: ENST00000449052.1:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly1635Gly
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

7-100365499-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365499
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365499
    reference: chr 7
allele count: 4
allele frequency: 3.32529719843711e-5
allele num: 120290
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4906C>G
  hgvsp: ENSP00000445943.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4906C>G
  hgvsp: ENSP00000425454.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4906C>G
  hgvsp: ENSP00000422208.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4906C>G
  hgvsp: ENSP00000422387.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4906C>G
  hgvsp: ENSP00000445091.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4906C>G
  hgvsp: ENSP00000444427.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4906C>G
  hgvsp: ENSP00000425200.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.637C>G
  hgvsp: ENSP00000441117.1:p.Arg213Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4906C>G
  hgvsp: ENSP00000421245.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4906C>G
  hgvsp: ENSP00000423579.1:p.Arg1636Gly
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1636Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

7-100365499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365499
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365499
    reference: chr 7
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4906C>T
  hgvsp: ENSP00000421245.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4906C>T
  hgvsp: ENSP00000445091.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4906C>T
  hgvsp: ENSP00000422387.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4906C>T
  hgvsp: ENSP00000422208.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4906C>T
  hgvsp: ENSP00000444427.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4906C>T
  hgvsp: ENSP00000425200.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4906C>T
  hgvsp: ENSP00000425454.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4906C>T
  hgvsp: ENSP00000423579.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4906C>T
  hgvsp: ENSP00000445943.1:p.Arg1636Trp
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.637C>T
  hgvsp: ENSP00000441117.1:p.Arg213Trp
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1636Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

7-100365500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365500
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365500
    reference: chr 7
allele count: 3
allele frequency: 2.494055833596595e-5
allele num: 120286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.638G>A
  hgvsp: ENSP00000441117.1:p.Arg213Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4907G>A
  hgvsp: ENSP00000425200.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4907G>A
  hgvsp: ENSP00000425454.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4907G>A
  hgvsp: ENSP00000422208.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4907G>A
  hgvsp: ENSP00000421245.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4907G>A
  hgvsp: ENSP00000445091.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4907G>A
  hgvsp: ENSP00000445943.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4907G>A
  hgvsp: ENSP00000422387.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4907G>A
  hgvsp: ENSP00000444427.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4907G>A
  hgvsp: ENSP00000423579.1:p.Arg1636Gln
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg1636Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

7-100365508-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365508
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365508
    reference: chr 7
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4915A>G
  hgvsp: ENSP00000421245.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4915A>G
  hgvsp: ENSP00000422208.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4915A>G
  hgvsp: ENSP00000444427.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4915A>G
  hgvsp: ENSP00000423579.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4915A>G
  hgvsp: ENSP00000445943.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4915A>G
  hgvsp: ENSP00000425454.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4915A>G
  hgvsp: ENSP00000425200.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4915A>G
  hgvsp: ENSP00000445091.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.646A>G
  hgvsp: ENSP00000441117.1:p.Ile216Val
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4915A>G
  hgvsp: ENSP00000422387.1:p.Ile1639Val
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile1639Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

7-100365509-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365509
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365509
    reference: chr 7
allele count: 407
allele frequency: 3.381634484363056e-3
allele num: 120356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4916T>C
  hgvsp: ENSP00000425454.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4916T>C
  hgvsp: ENSP00000445091.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4916T>C
  hgvsp: ENSP00000423579.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4916T>C
  hgvsp: ENSP00000445943.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4916T>C
  hgvsp: ENSP00000421245.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4916T>C
  hgvsp: ENSP00000422208.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4916T>C
  hgvsp: ENSP00000422387.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4916T>C
  hgvsp: ENSP00000425200.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.647T>C
  hgvsp: ENSP00000441117.1:p.Ile216Thr
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4916T>C
  hgvsp: ENSP00000444427.1:p.Ile1639Thr
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 19009
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 29781
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 1
hgvs: p.Ile1639Thr
num of homozygotes: 10
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

7-100365509-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365509
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365508
    reference: chr 7
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4918delA
  hgvsp: ENSP00000425200.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4918delA
  hgvsp: ENSP00000421245.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.649delA
  hgvsp: ENSP00000441117.1:p.Arg217GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4918delA
  hgvsp: ENSP00000445943.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4918delA
  hgvsp: ENSP00000425454.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4918delA
  hgvsp: ENSP00000445091.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4918delA
  hgvsp: ENSP00000422387.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4918delA
  hgvsp: ENSP00000422208.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4918delA
  hgvsp: ENSP00000444427.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4918delA
  hgvsp: ENSP00000423579.1:p.Arg1640GlyfsTer27
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1640GlyfsTer27
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: TA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-100365510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100365510
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100365510
    reference: chr 7
allele count: 2
allele frequency: 1.661819692563357e-5
allele num: 120350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425454
  ensembl transcript: ENST00000421100
  gene symbol: ZAN
  hgvsc: ENST00000421100.1:c.4917A>G
  hgvsp: ENSP00000425454.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445943
  ensembl transcript: ENST00000546292
  gene symbol: ZAN
  hgvsc: ENST00000546292.1:c.4917A>G
  hgvsp: ENSP00000445943.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000445091
  ensembl transcript: ENST00000538115
  gene symbol: ZAN
  hgvsc: ENST00000538115.1:c.4917A>G
  hgvsp: ENSP00000445091.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000425200
  ensembl transcript: ENST00000427578
  gene symbol: ZAN
  hgvsc: ENST00000427578.1:c.4917A>G
  hgvsp: ENSP00000425200.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000421245
  ensembl transcript: ENST00000443370
  gene symbol: ZAN
  hgvsc: ENST00000443370.1:c.4917A>G
  hgvsp: ENSP00000421245.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000444427
  ensembl transcript: ENST00000542585
  gene symbol: ZAN
  hgvsc: ENST00000542585.1:c.4917A>G
  hgvsp: ENSP00000444427.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000423579
  ensembl transcript: ENST00000348028
  gene symbol: ZAN
  hgvsc: ENST00000348028.3:c.4917A>G
  hgvsp: ENSP00000423579.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000441117
  ensembl transcript: ENST00000546213
  gene symbol: ZAN
  hgvsc: ENST00000546213.1:c.648A>G
  hgvsp: ENSP00000441117.1:p.Ile216Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422387
  ensembl transcript: ENST00000349350
  gene symbol: ZAN
  hgvsc: ENST00000349350.6:c.4917A>G
  hgvsp: ENSP00000422387.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146839
  ensembl protein: ENSP00000422208
  ensembl transcript: ENST00000449052
  gene symbol: ZAN
  hgvsc: ENST00000449052.1:c.4917A>G
  hgvsp: ENSP00000422208.1:p.Ile1639Met
  variant of: http://identifiers.org/hgnc/12857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile1639Met
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 5928
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13979
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3806
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2607
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4443
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.278e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 3.625e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.127e0

DP
type: SiteQuality
SIO_000300: 2.292198e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

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

GenotypeQuality
all individuals: 3805
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4445
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21821
bin: 9.75e1
variant carriers: 17

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

GenotypeQuality
all individuals: 2604
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5928
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4294
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.399016403274657e-4
allele num: 66694
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.259e1

FS
type: SiteQuality
SIO_000300: 2.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 2.292064e6

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.558e0

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

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

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

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

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

South Asian
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African
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allele frequency: 1.02082482645978e-4
allele num: 9796
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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

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

Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66696
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Other
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num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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East Asian
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Latino
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allele frequency: 8.644536652835408e-5
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num of homozygotes: 0

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

BaseQRankSum
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ClippingRankSum
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FS
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SIO_000300: 2.623e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

DP
type: SiteQuality
SIO_000300: 2.290057e6

VQSLOD
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SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

QD
type: SiteQuality
SIO_000300: 1.162e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

African
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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: 8620
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 4.8e-3

FS
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SIO_000300: 7.834e0

MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 1.36e-1

MQ
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SIO_000300: 5.989e1

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

DP
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SIO_000300: 2.289973e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.635e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.997660608241857e-5
allele num: 66684
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 3.0e-3

DP
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SIO_000300: 2.288393e6

BaseQRankSum
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SIO_000300: 2.69e0

VQSLOD
type: SiteQuality
SIO_000300: 9.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.259e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498830304120928e-5
allele num: 66684
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
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SIO_000300: 2.69e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.288393e6

InbreedingCoeff
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SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.259e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

DP
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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SIO_000300: 1.654e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.593e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
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allele frequency: 1.118568232662192e-3
allele num: 894
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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
allele num: 8616
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.062474479379339e-4
allele num: 9796
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

DP
type: SiteQuality
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.9e-3

GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.500180007200288e-5
allele num: 66664
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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East Asian
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allele count: 24
allele frequency: 2.785515320334262e-3
allele num: 8616
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MQ
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

East Asian
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European (Finnish)
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African
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allele frequency: 3.062474479379339e-4
allele num: 9796
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
SIO_000300: 5.3e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.049979000419992e-4
allele num: 66668
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 894
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

InbreedingCoeff
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SIO_000300: 3.6e-3

MQRankSum
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FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
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SIO_000300: -9.53e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

DP
type: SiteQuality
SIO_000300: 2.286223e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 1.196e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 4.9e-1

MQRankSum
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FS
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BaseQRankSum
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SIO_000300: 7.51e-1

VQSLOD
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QD
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SIO_000300: 9.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 2.285742e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.1e0

MQRankSum
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SIO_000300: 1.0e0

InbreedingCoeff
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SIO_000300: 4.5e-3

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 5.404e0

BaseQRankSum
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SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 2.285742e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002761270184285e-5
allele num: 66636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.591e1

FS
type: SiteQuality
SIO_000300: 3.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.11e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 2.285781e6

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

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

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.284433e6

QD
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FS
type: SiteQuality
SIO_000300: 1.1983e1

VQSLOD
type: SiteQuality
SIO_000300: -1.898e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

East Asian
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
allele num: 894
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: -3.582e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 260

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 2
allele frequency: 2.041649652919559e-4
allele num: 9796
num of homozygotes: 0

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

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

Other
type: Population
allele count: 2
allele frequency: 2.237136465324385e-3
allele num: 894
num of homozygotes: 0

South Asian
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allele count: 265
allele frequency: 1.604893410852713e-2
allele num: 16512
num of homozygotes: 8

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
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QD
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.27e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 3229
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 14092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21636
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 4402
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3796
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 1.940359477124183e-3
allele num: 9792
num of homozygotes: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 1.105e0

DP
type: SiteQuality
SIO_000300: 2.279331e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

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

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 135
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.216e1

MQRankSum
type: SiteQuality
SIO_000300: -2.92e-1

DP
type: SiteQuality
SIO_000300: 2.278322e6

FS
type: SiteQuality
SIO_000300: 4.522e0

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

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21610
bin: 9.75e1
variant carriers: 4

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50558692779046e-5
allele num: 66584
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 5.986e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 2.275173e6

QD
type: SiteQuality
SIO_000300: 1.252e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

MQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
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variant carriers: 0

GenotypeQuality
all individuals: 21608
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5796
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variant carriers: 0

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 14044
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
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variant carriers: 0

GenotypeQuality
all individuals: 4357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

FS
type: SiteQuality
SIO_000300: 1.6309e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.467e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.474e0

MQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

DP
type: SiteQuality
SIO_000300: 2.274903e6

QD
type: SiteQuality
SIO_000300: 6.61e0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 89
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 14078
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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: 4221
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 4347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21605
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5781
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 2.045408058907752e-4
allele num: 9778
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

DP
type: SiteQuality
SIO_000300: 2.273261e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.941e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.523e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

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

GenotypeQuality
all individuals: 21601
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006162633398467e-5
allele num: 66530
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.425418384671356e-4
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 1.131e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.276e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

DP
type: SiteQuality
SIO_000300: 2.27263e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 5710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 134
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GenotypeQuality
all individuals: 2576
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GenotypeQuality
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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: 13970
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variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.891e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 2.27042e6

QD
type: SiteQuality
SIO_000300: 1.176e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
all individuals: 75
bin: 3.75e1
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GenotypeQuality
all individuals: 4337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21593
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
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variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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East Asian
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Latino
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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QD
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MQRankSum
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BaseQRankSum
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DP
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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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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 frequency: 3.494060097833683e-4
allele num: 8586
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11544
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South Asian
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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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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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 frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

African
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allele frequency: 1.026061974143238e-4
allele num: 9746
num of homozygotes: 0

DP
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FS
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
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

Other
type: Population
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allele frequency: 1.128668171557562e-3
allele num: 886
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

FS
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MQ
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SIO_000300: 5.992e1

VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.4e-3

MQRankSum
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SIO_000300: 9.6e-2

DP
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ClippingRankSum
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SIO_000300: -5.600000000000001e-1

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
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East Asian
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allele count: 40
allele frequency: 4.670714619336758e-3
allele num: 8564
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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allele frequency: 0.0e0
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African
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allele num: 9588
num of homozygotes: 0

InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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Latino
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Other
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South Asian
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FS
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Latino
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MQ
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

European (Non-Finnish)
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allele count: 19
allele frequency: 2.958672023420225e-4
allele num: 64218
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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SIO_000300: 5.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -8.500000000000001e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 9496
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11422
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 (Non-Finnish)
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allele count: 1
allele frequency: 1.558749259594102e-5
allele num: 64154
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: -2.57e-1

ClippingRankSum
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DP
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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QD
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ReadPosRankSum
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SIO_000300: 1.4e0

VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 62858
num of homozygotes: 0

Latino
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allele frequency: 8.973438621679828e-5
allele num: 11144
num of homozygotes: 0

Other
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9290
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11148
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

African
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allele count: 1
allele frequency: 1.077354018530489e-4
allele num: 9282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62900
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: 8440
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

DP
type: SiteQuality
SIO_000300: 1.2799e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 6.016e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6482
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: 1.186802753382388e-4
allele num: 8426
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62768
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.807337791433219e-4
allele num: 11066
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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SIO_000300: 1.125e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQRankSum
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SIO_000300: -3.7e-2

InbreedingCoeff
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MQ
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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African
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allele num: 9352
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East Asian
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Other
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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MQRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.2e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8486
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Latino
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European (Finnish)
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South Asian
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ReadPosRankSum
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VQSLOD
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FS
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QD
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MQRankSum
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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Other
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.06473594548552e-4
allele num: 9392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.608e0

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.39853e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.417508417508418e-5
allele num: 11880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.403006e6

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.046e0

VQSLOD
type: SiteQuality
SIO_000300: -3.011e0

QD
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.123828564288392e-5
allele num: 64024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9482
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.347e0

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.189e0

DP
type: SiteQuality
SIO_000300: 1.430614e6

FS
type: SiteQuality
SIO_000300: 6.218e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.194e-1

QD
type: SiteQuality
SIO_000300: 7.8e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 32

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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variant carriers: 39

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 32

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 36

GenotypeQuality
all individuals: 309
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GenotypeQuality
all individuals: 7424
bin: 9.75e1
variant carriers: 4893

African
type: Population
allele count: 80
allele frequency: 8.40866092074837e-3
allele num: 9514
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3008
allele frequency: 4.67516319552378e-2
allele num: 64340
num of homozygotes: 84

East Asian
type: Population
allele count: 4
allele frequency: 4.664179104477612e-4
allele num: 8576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 263
allele frequency: 4.003044140030441e-2
allele num: 6570
num of homozygotes: 13

Latino
type: Population
allele count: 360
allele frequency: 3.169014084507042e-2
allele num: 11360
num of homozygotes: 6

Other
type: Population
allele count: 56
allele frequency: 6.845965770171149e-2
allele num: 818
num of homozygotes: 3

South Asian
type: Population
allele count: 1529
allele frequency: 1.168960244648318e-1
allele num: 13080
num of homozygotes: 79

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.17e0

FS
type: SiteQuality
SIO_000300: 1.639e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
type: SiteQuality
SIO_000300: 1.490131e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

QD
type: SiteQuality
SIO_000300: 1.404e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 1036
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3046
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GenotypeQuality
all individuals: 458
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550628004341758e-5
allele num: 64490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.222e0

MQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.469317e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 3060
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 1.535768037595602e-5
allele num: 65114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14252
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

FS
type: SiteQuality
SIO_000300: 9.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.50163e6

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 188
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65778
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.505334374186833e-5
allele num: 15372
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.334e0

MQ
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.01e0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65834
num of homozygotes: 0

Other
type: Population
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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: 8610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.848e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
all individuals: 1125
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GenotypeQuality
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GenotypeQuality
all individuals: 141
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 180
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.113831758665735e-5
allele num: 65834
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.436663233779608e-5
allele num: 15536
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.536588e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.848e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.74e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37540
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 3268
bin: 9.75e1
variant carriers: 215

GenotypeQuality
all individuals: 1062
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 13
allele frequency: 1.129060274448497e-3
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.272727272727273e-3
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.221311475409836e-4
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 182
allele frequency: 2.760754808567441e-3
allele num: 65924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.130081300813008e-4
allele num: 8610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.545762e6

VQSLOD
type: SiteQuality
SIO_000300: 6.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 3144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.5e0
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GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
all individuals: 1072
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GenotypeQuality
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GenotypeQuality
all individuals: 141
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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: 918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515243348081702e-5
allele num: 65996
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.93e-1

QD
type: SiteQuality
SIO_000300: 2.511e1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.544333e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.216e0

FS
type: SiteQuality
SIO_000300: 2.155e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 7900
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 1092
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 2068
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
all individuals: 38312
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variant carriers: 0

GenotypeQuality
all individuals: 2699
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variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66354
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.221597849987784e-4
allele num: 16372
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 3.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.64e-1

FS
type: SiteQuality
SIO_000300: 2.218e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.12e-1

DP
type: SiteQuality
SIO_000300: 1.5605e6

GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 2707
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 2073
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variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3119
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3202
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variant carriers: 0

GenotypeQuality
all individuals: 38423
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 8.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013046491307361e-5
allele num: 66378
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 7.45e0

VQSLOD
type: SiteQuality
SIO_000300: -1.318e0

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 9.196999999999999e0

DP
type: SiteQuality
SIO_000300: 1.560826e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 360
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GenotypeQuality
all individuals: 7903
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GenotypeQuality
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GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 2699
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 862
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 9.75e1
variant carriers: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.91e-1

DP
type: SiteQuality
SIO_000300: 1.56206e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

QD
type: SiteQuality
SIO_000300: 8.16e0

VQSLOD
type: SiteQuality
SIO_000300: -1.656e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 6.916e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2701
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 84
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 862
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GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
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variant carriers: 0

GenotypeQuality
all individuals: 38534
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 4
allele frequency: 4.092490280335584e-4
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.173e1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

DP
type: SiteQuality
SIO_000300: 1.562769e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7910
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505888022166672e-5
allele num: 66406
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

DP
type: SiteQuality
SIO_000300: 1.562769e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
all individuals: 2695
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 38523
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 865
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 3
allele frequency: 3.06873977086743e-4
allele num: 9776
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66400
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

FS
type: SiteQuality
SIO_000300: 3.296e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 1.203e1

DP
type: SiteQuality
SIO_000300: 1.563615e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38533
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 1.564258e6

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3485
bin: 9.75e1
variant carriers: 394

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38335
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 22
allele frequency: 1.905421791096484e-3
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.107291227647661e-4
allele num: 66436
num of homozygotes: 0

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

African
type: Population
allele count: 366
allele frequency: 3.741566141893273e-2
allele num: 9782
num of homozygotes: 10

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

Other
type: Population
allele count: 4
allele frequency: 4.474272930648769e-3
allele num: 894
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.84e-2

DP
type: SiteQuality
SIO_000300: 1.576608e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.384e1

GenotypeQuality
all individuals: 38335
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1086
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

QD
type: SiteQuality
SIO_000300: 1.384e1

DP
type: SiteQuality
SIO_000300: 1.576608e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2